부산대학교 도서관

B. Luzón-Toro; R. M. Fernández; J. M. Martos-Martínez; M. Rubio-Manzanares-Dorado; G. Antiñolo; S. Borrego

Sci Rep
RISalud-ANDALUCIA. Repositorio Institucional de Salud de Andalucía
instname
Digital.CSIC. Repositorio Institucional del CSIC
Consejo Superior de Investigaciones Científicas (CSIC)

M J B, Juárez; A, Zafra-Gómez; B, Luzón-Toro; O A, Ballesteros-García; A, Navalón; J, González; J L, Vílchez

Bioresource Technology. 99:2392-2398

Wirths, Oliver ; Thelen, Karin ; Breyhan, Henning ; Luzón-Toro, Berta ; Hoffmann, Karl-Heinz ; Falkai, Peter ; Lütjohann, Dieter ; Bayer, Thomas A.

In Experimental Gerontology 2006 41(2):220-224

Luzón-Toro, B; Gui, H; Tang, SM; Garcia-Barcelo, MM; Tam, PKH; Sham, PC; Cherny, SS

Mederer T; Department of Human Molecular Genetics, Heidelberg University Hospital, Heidelberg, Germany.; Schmitteckert S; Department of Human Molecular Genetics, Heidelberg University Hospital, Heidelberg, Germany.; Volz J; Department of Human Molecular Genetics, Heidelberg University Hospital, Heidelberg, Germany.; Martínez C; Department of Human Molecular Genetics, Heidelberg University Hospital, Heidelberg, Germany.; Lleida Institute for Biomedical Research Dr. Pifarré Foundation (IRBLleida), Lleida, Spain.; Röth R; Department of Human Molecular Genetics, Heidelberg University Hospital, Heidelberg, Germany.; nCounter Core Facility, Department of Human Molecular Genetics, Heidelberg University Hospital, Heidelberg, Germany.; Thumberger T; Centre for Organismal Studies, Heidelberg University, Heidelberg, Germany.; Eckstein V; FACS Core Facility, Campus Heidelberg, Germany.; Scheuerer J; Institute of Pathology, Heidelberg University Hospital, Heidelberg, Germany.; Thöni C; Institute of Pathology, Heidelberg University Hospital, Heidelberg, Germany.; Lasitschka F; Institute of Pathology, Heidelberg University Hospital, Heidelberg, Germany.; Carstensen L; Pediatric Surgery Division, Heidelberg University Hospital, Heidelberg, Germany.; Günther P; Pediatric Surgery Division, Heidelberg University Hospital, Heidelberg, Germany.; Holland-Cunz S; Pediatric Surgery, University Children's Hospital, Basel, Switzerland.; Hofstra R; Department of Clinical Genetics, Erasmus University Medical Center, Rotterdam, The Netherlands.; Brosens E; Department of Clinical Genetics, Erasmus University Medical Center, Rotterdam, The Netherlands.; Rosenfeld JA; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, United States of America.; Baylor Genetics Laboratories, Houston, Texas, United States of America.; Schaaf CP; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, United States of America.; Baylor Genetics Laboratories, Houston, Texas, United States of America.; Institute of Human Genetics, Heidelberg University Hospital, Heidelberg, Germany.; Schriemer D; Department of Neuroscience, University Medical Center, Groningen, The Netherlands.; Ceccherini I; UOSD Genetica e Genomica delle Malattie Rare, IRCCS, Instituto Giannina Gaslini, Genova, Italy.; Rusmini M; UOSD Genetica e Genomica delle Malattie Rare, IRCCS, Instituto Giannina Gaslini, Genova, Italy.; Tilghman J; Center for Human Genetics and Genomics, New York University School of Medicine, United States of America.; Luzón-Toro B; Department of Maternofetal Medicine, Genetics and Reproduction, Institute of Biomedicine of Seville (IBIS), University Hospital Virgen del Rocío/CSIC/University of Seville, Seville, Spain.; Centre for Biomedical Network Research on Rare Diseases (CIBERER), Seville, Spain.; Torroglosa A; Department of Maternofetal Medicine, Genetics and Reproduction, Institute of Biomedicine of Seville (IBIS), University Hospital Virgen del Rocío/CSIC/University of Seville, Seville, Spain.; Centre for Biomedical Network Research on Rare Diseases (CIBERER), Seville, Spain.; Borrego S; Department of Maternofetal Medicine, Genetics and Reproduction, Institute of Biomedicine of Seville (IBIS), University Hospital Virgen del Rocío/CSIC/University of Seville, Seville, Spain.; Centre for Biomedical Network Research on Rare Diseases (CIBERER), Seville, Spain.; Sze-Man Tang C; Department of Surgery, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, China.; Garcia-Barceló M; Department of Surgery, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, China.; Tam P; Department of Surgery, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, China.; Paramasivam N; Division of Theoretical Bioinformatics, German Cancer Research Center, Heidelberg, Germany.; Bewerunge-Hudler M; Genomics and Proteomic Core Facility, German Cancer Research Center, Heidelberg, Germany.; De La Torre C; Center of Medical Research, Medical Faculty Mannheim, Mannheim, Germany.; Gretz N; Center of Medical Research, Medical Faculty Mannheim, Mannheim, Germany.; Rappold GA; Department of Human Molecular Genetics, Heidelberg University Hospital, Heidelberg, Germany.; Interdisciplinary Center for Neurosciences, University of Heidelberg, Heidelberg, Germany.; Romero P; Pediatric Surgery Division, Heidelberg University Hospital, Heidelberg, Germany.; Niesler B; Department of Human Molecular Genetics, Heidelberg University Hospital, Heidelberg, Germany.; nCounter Core Facility, Department of Human Molecular Genetics, Heidelberg University Hospital, Heidelberg, Germany.; Interdisciplinary Center for Neurosciences, University of Heidelberg, Heidelberg, Germany.

Publisher: Public Library of Science Country of Publication: United States NLM ID: 101239074 Publication Model: eCollection Cited Medium: Internet ISSN: 1553-7404 (Electronic) Linking ISSN: 15537390 NLM ISO Abbreviation: PLoS Genet Subsets: MEDLINE

R. M. Fernández; M. Bleda; B. Luzón Toro; L. García Alonso; S. Arnold; Y. Sribudiani; C. Besmond; LANTIERI, FRANCESCA; B. Doan; I. Ceccherini; S. Lyonnet; R. M. Hofstra; A. Chakravarti; G. Antiñolo; J. Dopazo; S. Borrego

Orphanet J Rare Dis
Orphanet Journal of Rare Diseases
r-CIPF. Repositorio Institucional Producción Científica del Centro de Investigación Principe Felipe (CIPF)
instname
Digital.CSIC. Repositorio Institucional del CSIC
r-CIPF: Repositorio Institucional Producción Científica del Centro de Investigación Principe Felipe (CIPF)
Centro de Investigación Principe Felipe (CIPF)
idUS. Depósito de Investigación de la Universidad de Sevilla
Universidad de Sevilla (US)
idUS: Depósito de Investigación de la Universidad de Sevilla

Zafra-Gómez, A.; Luzón-Toro, B.; Jiménez-Diaz, I.; Ballesteros, O.; Navalón, A.

Journal of Pharmaceutical and Biomedical Analysis. Sep 01, 2010 53(1):103-108

Luzón-Toro B; Department of Maternofetal Medicine, Genetics and Reproduction, Institute of Biomedicine of Seville (IBIS), University Hospital Virgen del Rocío/CSIC, University of Seville, Seville, Spain.; Centre for Biomedical Network Research on Rare Diseases CIBERER, Seville, Spain.; Villalba-Benito L; Department of Maternofetal Medicine, Genetics and Reproduction, Institute of Biomedicine of Seville (IBIS), University Hospital Virgen del Rocío/CSIC, University of Seville, Seville, Spain.; Centre for Biomedical Network Research on Rare Diseases CIBERER, Seville, Spain.; Fernández RM; Department of Maternofetal Medicine, Genetics and Reproduction, Institute of Biomedicine of Seville (IBIS), University Hospital Virgen del Rocío/CSIC, University of Seville, Seville, Spain.; Centre for Biomedical Network Research on Rare Diseases CIBERER, Seville, Spain.; Torroglosa A; Department of Maternofetal Medicine, Genetics and Reproduction, Institute of Biomedicine of Seville (IBIS), University Hospital Virgen del Rocío/CSIC, University of Seville, Seville, Spain.; Centre for Biomedical Network Research on Rare Diseases CIBERER, Seville, Spain.; Antiñolo G; Department of Maternofetal Medicine, Genetics and Reproduction, Institute of Biomedicine of Seville (IBIS), University Hospital Virgen del Rocío/CSIC, University of Seville, Seville, Spain.; Centre for Biomedical Network Research on Rare Diseases CIBERER, Seville, Spain.; Borrego S; Department of Maternofetal Medicine, Genetics and Reproduction, Institute of Biomedicine of Seville (IBIS), University Hospital Virgen del Rocío/CSIC, University of Seville, Seville, Spain. salud.borrego.sspa@juntadeandalucia.es.; Centre for Biomedical Network Research on Rare Diseases CIBERER, Seville, Spain. salud.borrego.sspa@juntadeandalucia.es.

Publisher: BioMed Central Country of Publication: England NLM ID: 101266602 Publication Model: Electronic Cited Medium: Internet ISSN: 1750-1172 (Electronic) Linking ISSN: 17501172 NLM ISO Abbreviation: Orphanet J Rare Dis Subsets: MEDLINE

Luzón-Toro B; Department of Maternofetal Medicine, Genetics and Reproduction, Institute of Biomedicine of Seville (IBIS), University Hospital Virgen del Rocío/CSIC/University of Seville, Seville, Spain.; Centre for Biomedical Network Research on Rare Diseases (CIBERER), Seville, Spain.; Villalba-Benito L; Department of Maternofetal Medicine, Genetics and Reproduction, Institute of Biomedicine of Seville (IBIS), University Hospital Virgen del Rocío/CSIC/University of Seville, Seville, Spain.; Centre for Biomedical Network Research on Rare Diseases (CIBERER), Seville, Spain.; Torroglosa A; Department of Maternofetal Medicine, Genetics and Reproduction, Institute of Biomedicine of Seville (IBIS), University Hospital Virgen del Rocío/CSIC/University of Seville, Seville, Spain.; Centre for Biomedical Network Research on Rare Diseases (CIBERER), Seville, Spain.; Fernández RM; Department of Maternofetal Medicine, Genetics and Reproduction, Institute of Biomedicine of Seville (IBIS), University Hospital Virgen del Rocío/CSIC/University of Seville, Seville, Spain.; Centre for Biomedical Network Research on Rare Diseases (CIBERER), Seville, Spain.; Antiñolo G; Department of Maternofetal Medicine, Genetics and Reproduction, Institute of Biomedicine of Seville (IBIS), University Hospital Virgen del Rocío/CSIC/University of Seville, Seville, Spain.; Centre for Biomedical Network Research on Rare Diseases (CIBERER), Seville, Spain.; Borrego S; Department of Maternofetal Medicine, Genetics and Reproduction, Institute of Biomedicine of Seville (IBIS), University Hospital Virgen del Rocío/CSIC/University of Seville, Seville, Spain.; Centre for Biomedical Network Research on Rare Diseases (CIBERER), Seville, Spain.

Publisher: Munksgaard Country of Publication: Denmark NLM ID: 0253664 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1399-0004 (Electronic) Linking ISSN: 00099163 NLM ISO Abbreviation: Clin Genet Subsets: MEDLINE

Luzón-Toro B; Department of Maternofetal Medicine, Genetics and Reproduction, Institute of Biomedicine of Seville (IBIS), University Hospital Virgen del Rocío/CSIC/University of Seville, 41013 Seville, Spain.; Centre for Biomedical Network Research on Rare Diseases (CIBERER), 41013 Seville, Spain.; Fernández RM; Department of Maternofetal Medicine, Genetics and Reproduction, Institute of Biomedicine of Seville (IBIS), University Hospital Virgen del Rocío/CSIC/University of Seville, 41013 Seville, Spain.; Centre for Biomedical Network Research on Rare Diseases (CIBERER), 41013 Seville, Spain.; Villalba-Benito L; Department of Maternofetal Medicine, Genetics and Reproduction, Institute of Biomedicine of Seville (IBIS), University Hospital Virgen del Rocío/CSIC/University of Seville, 41013 Seville, Spain.; Centre for Biomedical Network Research on Rare Diseases (CIBERER), 41013 Seville, Spain.; Torroglosa A; Department of Maternofetal Medicine, Genetics and Reproduction, Institute of Biomedicine of Seville (IBIS), University Hospital Virgen del Rocío/CSIC/University of Seville, 41013 Seville, Spain.; Centre for Biomedical Network Research on Rare Diseases (CIBERER), 41013 Seville, Spain.; Antiñolo G; Department of Maternofetal Medicine, Genetics and Reproduction, Institute of Biomedicine of Seville (IBIS), University Hospital Virgen del Rocío/CSIC/University of Seville, 41013 Seville, Spain.; Centre for Biomedical Network Research on Rare Diseases (CIBERER), 41013 Seville, Spain.; Borrego S; Department of Maternofetal Medicine, Genetics and Reproduction, Institute of Biomedicine of Seville (IBIS), University Hospital Virgen del Rocío/CSIC/University of Seville, 41013 Seville, Spain.; Centre for Biomedical Network Research on Rare Diseases (CIBERER), 41013 Seville, Spain.

Publisher: MDPI Country of Publication: Switzerland NLM ID: 101551097 Publication Model: Electronic Cited Medium: Internet ISSN: 2073-4425 (Electronic) Linking ISSN: 20734425 NLM ISO Abbreviation: Genes (Basel) Subsets: MEDLINE

Gui H; Department of Surgery, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, SAR, China.; Centre for Genomic Sciences, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, SAR, China.; Schriemer D; Department of Neuroscience, section Medical Physiology, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.; Cheng WW; Department of Surgery, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, SAR, China.; Department of Clinical Genetics, Erasmus University Medical Center, PO Box 2040, 3000CA, Rotterdam, The Netherlands.; Chauhan RK; Department of Clinical Genetics, Erasmus University Medical Center, PO Box 2040, 3000CA, Rotterdam, The Netherlands.; Antiňolo G; Department of Genetics, Reproduction and Fetal Medicine, Institute of Biomedicine of Seville (IBIS), University Hospital Virgen del Rocío/CSIC/University of Seville, Seville, Spain.; Centre for Biomedical Network Research on Rare Diseases (CIBERER), Seville, Spain.; Berrios C; McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, USA.; Bleda M; Centre for Biomedical Network Research on Rare Diseases (CIBERER), Seville, Spain.; Department of Medicine, School of Clinical Medicine, University of Cambridge, Addenbrooke's Hospital, Cambridge, UK.; Brooks AS; Department of Clinical Genetics, Erasmus University Medical Center, PO Box 2040, 3000CA, Rotterdam, The Netherlands.; Brouwer RW; Erasmus Center for Biomics, Erasmus Medical Center, Rotterdam, The Netherlands.; Burns AJ; Department of Clinical Genetics, Erasmus University Medical Center, PO Box 2040, 3000CA, Rotterdam, The Netherlands.; Stem Cells and Regenerative Medicine, Birth Defects Research Centre, UCL Institute of Child Health, London, UK.; Cherny SS; Centre for Genomic Sciences, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, SAR, China.; Dopazo J; Department of Genetics, Reproduction and Fetal Medicine, Institute of Biomedicine of Seville (IBIS), University Hospital Virgen del Rocío/CSIC/University of Seville, Seville, Spain.; Centre for Biomedical Network Research on Rare Diseases (CIBERER), Seville, Spain.; Eggen BJ; Department of Neuroscience, section Medical Physiology, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.; Griseri P; UOC Genetica Medica, Istituto Gaslini, Genoa, Italy.; Jalloh B; Department of Biology, Emory University, Atlanta, USA.; Le TL; Laboratory of embryology and genetics of human malformations, INSERM UMR 1163, Institut Imagine, Paris, France.; Department of Genetics, Paris Descartes-Sorbonne Paris Cité University, Hôpital Necker-Enfants Malades (APHP), Paris, France.; Lui VC; Department of Surgery, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, SAR, China.; Luzón-Toro B; Department of Genetics, Reproduction and Fetal Medicine, Institute of Biomedicine of Seville (IBIS), University Hospital Virgen del Rocío/CSIC/University of Seville, Seville, Spain.; Centre for Biomedical Network Research on Rare Diseases (CIBERER), Seville, Spain.; Matera I; UOC Genetica Medica, Istituto Gaslini, Genoa, Italy.; Ngan ES; Department of Surgery, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, SAR, China.; Pelet A; Laboratory of embryology and genetics of human malformations, INSERM UMR 1163, Institut Imagine, Paris, France.; Department of Genetics, Paris Descartes-Sorbonne Paris Cité University, Hôpital Necker-Enfants Malades (APHP), Paris, France.; Ruiz-Ferrer M; Department of Genetics, Reproduction and Fetal Medicine, Institute of Biomedicine of Seville (IBIS), University Hospital Virgen del Rocío/CSIC/University of Seville, Seville, Spain.; Centre for Biomedical Network Research on Rare Diseases (CIBERER), Seville, Spain.; Sham PC; Centre for Genomic Sciences, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, SAR, China.; Shepherd IT; Department of Biology, Emory University, Atlanta, USA.; So MT; Department of Surgery, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, SAR, China.; Sribudiani Y; Department of Clinical Genetics, Erasmus University Medical Center, PO Box 2040, 3000CA, Rotterdam, The Netherlands.; Department of Biochemistry and Molecular Biology, Faculty of Medicine, Universitas Padjadjaran, Bandung, Indonesia.; Tang CS; Department of Surgery, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, SAR, China.; van den Hout MC; Erasmus Center for Biomics, Erasmus Medical Center, Rotterdam, The Netherlands.; van der Linde HC; Department of Clinical Genetics, Erasmus University Medical Center, PO Box 2040, 3000CA, Rotterdam, The Netherlands.; van Ham TJ; Department of Clinical Genetics, Erasmus University Medical Center, PO Box 2040, 3000CA, Rotterdam, The Netherlands.; van IJcken WF; Erasmus Center for Biomics, Erasmus Medical Center, Rotterdam, The Netherlands.; Verheij JB; Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.; Amiel J; Laboratory of embryology and genetics of human malformations, INSERM UMR 1163, Institut Imagine, Paris, France.; Department of Genetics, Paris Descartes-Sorbonne Paris Cité University, Hôpital Necker-Enfants Malades (APHP), Paris, France.; Borrego S; Department of Genetics, Reproduction and Fetal Medicine, Institute of Biomedicine of Seville (IBIS), University Hospital Virgen del Rocío/CSIC/University of Seville, Seville, Spain.; Centre for Biomedical Network Research on Rare Diseases (CIBERER), Seville, Spain.; Ceccherini I; UOC Genetica Medica, Istituto Gaslini, Genoa, Italy.; Chakravarti A; McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, USA.; Lyonnet S; Laboratory of embryology and genetics of human malformations, INSERM UMR 1163, Institut Imagine, Paris, France.; Department of Genetics, Paris Descartes-Sorbonne Paris Cité University, Hôpital Necker-Enfants Malades (APHP), Paris, France.; Tam PK; Department of Surgery, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, SAR, China.; Garcia-Barceló MM; Department of Surgery, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, SAR, China. mmgarcia@hku.hk.; Hofstra RM; Department of Clinical Genetics, Erasmus University Medical Center, PO Box 2040, 3000CA, Rotterdam, The Netherlands. r.hofstra@erasmusmc.nl.; Stem Cells and Regenerative Medicine, Birth Defects Research Centre, UCL Institute of Child Health, London, UK. r.hofstra@erasmusmc.nl.

Publisher: BioMed Central Ltd Country of Publication: England NLM ID: 100960660 Publication Model: Electronic Cited Medium: Internet ISSN: 1474-760X (Electronic) Linking ISSN: 14747596 NLM ISO Abbreviation: Genome Biol Subsets: MEDLINE

Villalba-Benito, L.; Torroglosa, A.; Luzón-Toro, B.; Fernández, R.M.; Antiñolo, G.; Borrego, S.; Dopazo, J.; López-López, D.; Casimiro-Soriguer, C.S.; Moya-Jiménez, M.J.

In: Clinical Epigenetics. (Clinical Epigenetics, December 2021, 13(1))

Tang CS; Department of Surgery.; Centre for Genomic Sciences.; Dr Li Dak-Sum Research Centre, The University of Hong Kong - Karolinska Institutet Collaboration in Regenerative Medicine, Hong Kong SAR, China.; Gui H; Department of Surgery.; Centre for Genomic Sciences.; Kapoor A; Center for Complex Disease Genomics, McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.; Kim JH; Research Institute for Basic Science, Sogang University, Seoul 121-742, Republic of Korea.; Luzón-Toro B; Department of Genetics, Reproduction and Fetal Medicine, Institute of Biomedicine of Seville (IBIS), University Hospital Virgen del Rocío/CSIC/University of Seville, Seville, Spain.; Centre for Biomedical Network Research on Rare Diseases (CIBERER), Seville, Spain.; Pelet A; Laboratory of Embryology and Genetics of Congenital Malformations, Institut National de la Santé et de la Recherche Médicale (INSERM) U1163, Institut Imagine, Paris, France.; Paris Descartes-Sorbonne Paris Cité University, Institut Imagine, Paris, France.; Burzynski G; Department of Clinical Genetic, Erasmus Medical Center, Rotterdam, The Netherlands.; Lantieri F; UOC Genetica Medica, Istituto Giannina Gaslini, 16148 Genova, Italy.; So MT; Department of Surgery.; Berrios C; Center for Complex Disease Genomics, McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.; Shin HD; Research Institute for Basic Science, Sogang University, Seoul 121-742, Republic of Korea.; Department of Life Science, Sogang University, Seoul 121-742, Republic of Korea.; Fernández RM; Department of Genetics, Reproduction and Fetal Medicine, Institute of Biomedicine of Seville (IBIS), University Hospital Virgen del Rocío/CSIC/University of Seville, Seville, Spain.; Centre for Biomedical Network Research on Rare Diseases (CIBERER), Seville, Spain.; Le TL; Laboratory of Embryology and Genetics of Congenital Malformations, Institut National de la Santé et de la Recherche Médicale (INSERM) U1163, Institut Imagine, Paris, France.; Paris Descartes-Sorbonne Paris Cité University, Institut Imagine, Paris, France.; Verheij JB; Department of Clinical Genetic, Erasmus Medical Center, Rotterdam, The Netherlands.; Matera I; UOC Genetica Medica, Istituto Giannina Gaslini, 16148 Genova, Italy.; Cherny SS; Centre for Genomic Sciences.; Department of Psychiatry.; State Key Laboratory of Brain and Cognitive Sciences, The University of Hong Kong, Pokfulam, Hong Kong SAR, China.; Nandakumar P; Center for Complex Disease Genomics, McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.; Cheong HS; Department of Genetic Epidemiology, SNP Genetics, Inc., Seoul 121-742, Republic of Korea.; Antiñolo G; Department of Genetics, Reproduction and Fetal Medicine, Institute of Biomedicine of Seville (IBIS), University Hospital Virgen del Rocío/CSIC/University of Seville, Seville, Spain.; Centre for Biomedical Network Research on Rare Diseases (CIBERER), Seville, Spain.; Amiel J; Laboratory of Embryology and Genetics of Congenital Malformations, Institut National de la Santé et de la Recherche Médicale (INSERM) U1163, Institut Imagine, Paris, France.; Paris Descartes-Sorbonne Paris Cité University, Institut Imagine, Paris, France.; Seo JM; Division of Pediatric Surgery, Department of Surgery, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul 135-710, Republic of Korea.; Kim DY; Department of Pediatric Surgery, Asan Medical Center, University of Ulsan College of Medicine, Seoul 138-736, Republic of Korea.; Oh JT; Department of Pediatric Surgery, Severance Children's Hospital, Yonsei University College of Medicine, Seoul 120-752, Republic of Korea.; Lyonnet S; Laboratory of Embryology and Genetics of Congenital Malformations, Institut National de la Santé et de la Recherche Médicale (INSERM) U1163, Institut Imagine, Paris, France.; Paris Descartes-Sorbonne Paris Cité University, Institut Imagine, Paris, France.; Borrego S; Department of Genetics, Reproduction and Fetal Medicine, Institute of Biomedicine of Seville (IBIS), University Hospital Virgen del Rocío/CSIC/University of Seville, Seville, Spain.; Centre for Biomedical Network Research on Rare Diseases (CIBERER), Seville, Spain.; Ceccherini I; UOC Genetica Medica, Istituto Giannina Gaslini, 16148 Genova, Italy.; Hofstra RM; Department of Clinical Genetic, Erasmus Medical Center, Rotterdam, The Netherlands.; Stem Cells and Regenerative Medicine, Birth Defects Research Centre UCL Institute of Child Health, London, UK.; Chakravarti A; Center for Complex Disease Genomics, McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.; Kim HY; Department of Pediatric Surgery, Seoul National University Children's Hospital, Seoul 110-744, Republic of Korea.; Sham PC; Centre for Genomic Sciences.; Department of Psychiatry.; State Key Laboratory of Brain and Cognitive Sciences, The University of Hong Kong, Pokfulam, Hong Kong SAR, China.; Tam PK; Department of Surgery.; Dr Li Dak-Sum Research Centre, The University of Hong Kong - Karolinska Institutet Collaboration in Regenerative Medicine, Hong Kong SAR, China.; Garcia-Barceló MM; Department of Surgery.; Centre for Genomic Sciences.

Publisher: IRL Press at Oxford University Press Country of Publication: England NLM ID: 9208958 Publication Model: Print Cited Medium: Internet ISSN: 1460-2083 (Electronic) Linking ISSN: 09646906 NLM ISO Abbreviation: Hum Mol Genet Subsets: MEDLINE

Luzón-Toro B; Department of Genetics, Reproduction and Fetal Medicine, Institute of Biomedicine of Seville (IBIS), University Hospital Virgen del Rocío/CSIC/University of Seville, Seville, Spain. berta.luzon.exts@juntadeandalucia.es.; Centre for Biomedical Network Research on Rare Diseases (CIBERER), Seville, Spain. berta.luzon.exts@juntadeandalucia.es.; Bleda M; Centre for Biomedical Network Research on Rare Diseases (CIBERER), Seville, Spain. mb2033@cam.ac.uk.; Computational Genomics Department, Centro de Investigación Príncipe Felipe (CIPF), C/Eduardo Primo Yúfera, 3, 46012, Valencia, Spain. mb2033@cam.ac.uk.; Present Address: Department of Medicine, University of Cambridge, School of Clinical Medicine, Addenbrooke's Hospital, Hills Road, Cambridge, UK. mb2033@cam.ac.uk.; Navarro E; Centre for Biomedical Network Research on Rare Diseases (CIBERER), Seville, Spain. elena.navarro.sspa@juntadeandalucia.es.; Department of Endocrinology, Institute of Biomedicine of Seville (IBIS), University Hospital Virgen del Rocío/CSIC/University of Seville, Seville, Spain. elena.navarro.sspa@juntadeandalucia.es.; García-Alonso L; Computational Genomics Department, Centro de Investigación Príncipe Felipe (CIPF), C/Eduardo Primo Yúfera, 3, 46012, Valencia, Spain. luzgaral@ebi.ac.uk.; Present Address: European Bioinformatics Institute (EMBL-EBI), European Molecular Biology Laboratory, Wellcome Trust Genome Campus, Hinxton, Cambridge, UK. luzgaral@ebi.ac.uk.; Ruiz-Ferrer M; Department of Genetics, Reproduction and Fetal Medicine, Institute of Biomedicine of Seville (IBIS), University Hospital Virgen del Rocío/CSIC/University of Seville, Seville, Spain. mm.ruiz.exts@juntadeandalucia.es.; Centre for Biomedical Network Research on Rare Diseases (CIBERER), Seville, Spain. mm.ruiz.exts@juntadeandalucia.es.; Medina I; Computational Genomics Department, Centro de Investigación Príncipe Felipe (CIPF), C/Eduardo Primo Yúfera, 3, 46012, Valencia, Spain. im411@cam.ac.uk.; Present Address: HPC Services, University of Cambridge, Cambridge, UK. im411@cam.ac.uk.; Martín-Sánchez M; Department of Genetics, Reproduction and Fetal Medicine, Institute of Biomedicine of Seville (IBIS), University Hospital Virgen del Rocío/CSIC/University of Seville, Seville, Spain. martamartin-ibis@us.es.; Centre for Biomedical Network Research on Rare Diseases (CIBERER), Seville, Spain. martamartin-ibis@us.es.; Gonzalez CY; Computational Genomics Department, Centro de Investigación Príncipe Felipe (CIPF), C/Eduardo Primo Yúfera, 3, 46012, Valencia, Spain. cyenyxe@ebi.ac.uk.; Present Address: European Bioinformatics Institute (EMBL-EBI), European Molecular Biology Laboratory, Wellcome Trust Genome Campus, Hinxton, Cambridge, UK. cyenyxe@ebi.ac.uk.; Fernández RM; Department of Genetics, Reproduction and Fetal Medicine, Institute of Biomedicine of Seville (IBIS), University Hospital Virgen del Rocío/CSIC/University of Seville, Seville, Spain. raquelm.fernandez.sspa@juntadeandalucia.es.; Centre for Biomedical Network Research on Rare Diseases (CIBERER), Seville, Spain. raquelm.fernandez.sspa@juntadeandalucia.es.; Torroglosa A; Department of Genetics, Reproduction and Fetal Medicine, Institute of Biomedicine of Seville (IBIS), University Hospital Virgen del Rocío/CSIC/University of Seville, Seville, Spain. ana.torroglosa.exts@juntadeandalucia.es.; Centre for Biomedical Network Research on Rare Diseases (CIBERER), Seville, Spain. ana.torroglosa.exts@juntadeandalucia.es.; Antiñolo G; Department of Genetics, Reproduction and Fetal Medicine, Institute of Biomedicine of Seville (IBIS), University Hospital Virgen del Rocío/CSIC/University of Seville, Seville, Spain. guillermo.antinolo.sspa@juntadeandalucia.es.; Centre for Biomedical Network Research on Rare Diseases (CIBERER), Seville, Spain. guillermo.antinolo.sspa@juntadeandalucia.es.; Dopazo J; Centre for Biomedical Network Research on Rare Diseases (CIBERER), Seville, Spain. jdopazo@cipf.es.; Computational Genomics Department, Centro de Investigación Príncipe Felipe (CIPF), C/Eduardo Primo Yúfera, 3, 46012, Valencia, Spain. jdopazo@cipf.es.; Functional Genomics Node, (INB) at CIPF, Valencia, Spain. jdopazo@cipf.es.; Borrego S; Department of Genetics, Reproduction and Fetal Medicine, Institute of Biomedicine of Seville (IBIS), University Hospital Virgen del Rocío/CSIC/University of Seville, Seville, Spain. salud.borrego.sspa@juntadeandalucia.es.; Centre for Biomedical Network Research on Rare Diseases (CIBERER), Seville, Spain. salud.borrego.sspa@juntadeandalucia.es.

Publisher: BioMed Central Country of Publication: England NLM ID: 101319628 Publication Model: Electronic Cited Medium: Internet ISSN: 1755-8794 (Electronic) Linking ISSN: 17558794 NLM ISO Abbreviation: BMC Med Genomics Subsets: MEDLINE

Luzón-Toro B; Department of Genetics, Reproduction and Fetal Medicine, Institute of Biomedicine of Seville (IBIS), University Hospital Virgen del Rocío/CSIC/University of Seville, Seville, Spain. berta.luzon.exts@juntadeandalucia.es.; Centre for Biomedical Network Research on Rare Diseases (CIBERER), Seville, Spain. berta.luzon.exts@juntadeandalucia.es.; Espino-Paisán L; Department of Genetics, Reproduction and Fetal Medicine, Institute of Biomedicine of Seville (IBIS), University Hospital Virgen del Rocío/CSIC/University of Seville, Seville, Spain. laura.espino.exts@juntadeandalucia.es.; Centre for Biomedical Network Research on Rare Diseases (CIBERER), Seville, Spain. laura.espino.exts@juntadeandalucia.es.; Fernández RM; Department of Genetics, Reproduction and Fetal Medicine, Institute of Biomedicine of Seville (IBIS), University Hospital Virgen del Rocío/CSIC/University of Seville, Seville, Spain. raquelm.fernandez.sspa@juntadeandalucia.es.; Centre for Biomedical Network Research on Rare Diseases (CIBERER), Seville, Spain. raquelm.fernandez.sspa@juntadeandalucia.es.; Martín-Sánchez M; Department of Genetics, Reproduction and Fetal Medicine, Institute of Biomedicine of Seville (IBIS), University Hospital Virgen del Rocío/CSIC/University of Seville, Seville, Spain. m.martin.s@hotmail.com.; Centre for Biomedical Network Research on Rare Diseases (CIBERER), Seville, Spain. m.martin.s@hotmail.com.; Antiñolo G; Department of Genetics, Reproduction and Fetal Medicine, Institute of Biomedicine of Seville (IBIS), University Hospital Virgen del Rocío/CSIC/University of Seville, Seville, Spain. guillermo.antinolo.sspa@juntadeandalucia.es.; Centre for Biomedical Network Research on Rare Diseases (CIBERER), Seville, Spain. guillermo.antinolo.sspa@juntadeandalucia.es.; Borrego S; Department of Genetics, Reproduction and Fetal Medicine, Institute of Biomedicine of Seville (IBIS), University Hospital Virgen del Rocío/CSIC/University of Seville, Seville, Spain. salud.borrego.sspa@juntadeandalucia.es.; Centre for Biomedical Network Research on Rare Diseases (CIBERER), Seville, Spain. salud.borrego.sspa@juntadeandalucia.es.

Publisher: BioMed Central Country of Publication: England NLM ID: 100968552 Publication Model: Electronic Cited Medium: Internet ISSN: 1471-2350 (Electronic) Linking ISSN: 14712350 NLM ISO Abbreviation: BMC Med Genet Subsets: MEDLINE

Villalba-Benito L; Department of Maternofetal Medicine, Genetics and Reproduction, Institute of Biomedicine of Seville (IBIS), University Hospital Virgen del Rocío/CSIC/University of Seville, 41013 Seville, Spain.; Centre for Biomedical Network Research on Rare Diseases (CIBERER), 41013 Seville, Spain.; Torroglosa A; Department of Maternofetal Medicine, Genetics and Reproduction, Institute of Biomedicine of Seville (IBIS), University Hospital Virgen del Rocío/CSIC/University of Seville, 41013 Seville, Spain.; Centre for Biomedical Network Research on Rare Diseases (CIBERER), 41013 Seville, Spain.; Luzón-Toro B; Department of Maternofetal Medicine, Genetics and Reproduction, Institute of Biomedicine of Seville (IBIS), University Hospital Virgen del Rocío/CSIC/University of Seville, 41013 Seville, Spain.; Centre for Biomedical Network Research on Rare Diseases (CIBERER), 41013 Seville, Spain.; Fernández RM; Department of Maternofetal Medicine, Genetics and Reproduction, Institute of Biomedicine of Seville (IBIS), University Hospital Virgen del Rocío/CSIC/University of Seville, 41013 Seville, Spain.; Centre for Biomedical Network Research on Rare Diseases (CIBERER), 41013 Seville, Spain.; Moya-Jiménez MJ; Department of Pediatric Surgery, University Hospital Virgen del Rocío, 41013 Seville, Spain.; Antiñolo G; Department of Maternofetal Medicine, Genetics and Reproduction, Institute of Biomedicine of Seville (IBIS), University Hospital Virgen del Rocío/CSIC/University of Seville, 41013 Seville, Spain.; Centre for Biomedical Network Research on Rare Diseases (CIBERER), 41013 Seville, Spain.; Borrego S; Department of Maternofetal Medicine, Genetics and Reproduction, Institute of Biomedicine of Seville (IBIS), University Hospital Virgen del Rocío/CSIC/University of Seville, 41013 Seville, Spain.; Centre for Biomedical Network Research on Rare Diseases (CIBERER), 41013 Seville, Spain.

Publisher: MDPI Country of Publication: Switzerland NLM ID: 101092791 Publication Model: Electronic Cited Medium: Internet ISSN: 1422-0067 (Electronic) Linking ISSN: 14220067 NLM ISO Abbreviation: Int J Mol Sci Subsets: MEDLINE

Torroglosa A; Department of Maternofetal Medicine, Genetics and Reproduction, Institute of Biomedicine of Seville (IBIS), University Hospital Virgen del Rocío/CSIC/University of Seville, 41013 Seville, Spain.; Centre for Biomedical Network Research on Rare Diseases (CIBERER), 41013 Seville, Spain.; Villalba-Benito L; Department of Maternofetal Medicine, Genetics and Reproduction, Institute of Biomedicine of Seville (IBIS), University Hospital Virgen del Rocío/CSIC/University of Seville, 41013 Seville, Spain.; Centre for Biomedical Network Research on Rare Diseases (CIBERER), 41013 Seville, Spain.; Fernández RM; Department of Maternofetal Medicine, Genetics and Reproduction, Institute of Biomedicine of Seville (IBIS), University Hospital Virgen del Rocío/CSIC/University of Seville, 41013 Seville, Spain.; Centre for Biomedical Network Research on Rare Diseases (CIBERER), 41013 Seville, Spain.; Luzón-Toro B; Department of Maternofetal Medicine, Genetics and Reproduction, Institute of Biomedicine of Seville (IBIS), University Hospital Virgen del Rocío/CSIC/University of Seville, 41013 Seville, Spain.; Centre for Biomedical Network Research on Rare Diseases (CIBERER), 41013 Seville, Spain.; Moya-Jiménez MJ; Department of Pediatric Surgery, University Hospital Virgen del Rocío, 41013 Seville, Spain.; Antiñolo G; Department of Maternofetal Medicine, Genetics and Reproduction, Institute of Biomedicine of Seville (IBIS), University Hospital Virgen del Rocío/CSIC/University of Seville, 41013 Seville, Spain.; Centre for Biomedical Network Research on Rare Diseases (CIBERER), 41013 Seville, Spain.; Borrego S; Department of Maternofetal Medicine, Genetics and Reproduction, Institute of Biomedicine of Seville (IBIS), University Hospital Virgen del Rocío/CSIC/University of Seville, 41013 Seville, Spain.; Centre for Biomedical Network Research on Rare Diseases (CIBERER), 41013 Seville, Spain.

Publisher: MDPI Country of Publication: Switzerland NLM ID: 101092791 Publication Model: Electronic Cited Medium: Internet ISSN: 1422-0067 (Electronic) Linking ISSN: 14220067 NLM ISO Abbreviation: Int J Mol Sci Subsets: MEDLINE

Fernández RM; Department of Genetics, Reproduction and Fetal Medicine, Institute of Biomedicine of Seville, University Hospital Virgen del Rocío/Centro Superior de Investigaciones Científicas/University of Seville, Seville, Spain.; Mathieu Y; Luzón-Toro B; Núñez-Torres R; González-Meneses A; Antiñolo G; Amiel J; Borrego S

Publisher: Public Library of Science Country of Publication: United States NLM ID: 101285081 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1932-6203 (Electronic) Linking ISSN: 19326203 NLM ISO Abbreviation: PLoS One Subsets: MEDLINE

Luzón-Toro B; Department of Genetics, Reproduction and Fetal Medicine, Institute of Biomedicine of Seville, University Hospital Virgen del Rocío/Consejo Superior de Investigaciones Científicas/University of Seville, Seville, Spain.; Fernández RM; Torroglosa A; de Agustín JC; Méndez-Vidal C; Segura DI; Antiñolo G; Borrego S

Publisher: Public Library of Science Country of Publication: United States NLM ID: 101285081 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1932-6203 (Electronic) Linking ISSN: 19326203 NLM ISO Abbreviation: PLoS One Subsets: MEDLINE

Fernández RM; Department of Genetics, Reproduction and Fetal Medicine, Institute of Biomedicine of Seville (IBIS, University Hospital Virgen del Rocío/CSIC/University of Seville, Seville, Spain.; Bleda M; Núñez-Torres R; Medina I; Luzón-Toro B; García-Alonso L; Torroglosa A; Marbà M; Enguix-Riego MV; Montaner D; Antiñolo G; Dopazo J; Borrego S

Publisher: BioMed Central Country of Publication: England NLM ID: 101266602 Publication Model: Electronic Cited Medium: Internet ISSN: 1750-1172 (Electronic) Linking ISSN: 17501172 NLM ISO Abbreviation: Orphanet J Rare Dis Subsets: MEDLINE