부산대학교 도서관

Bryant, Laura; Li, Dong; Sherr, Elliott; Thompson, Michelle L; McWalter, Kirsty; Stumpel, Constance T R M; Stevens, Servi J C; Stegmann, Alexander P A; Tveten, Kristian; Vøllo, Arve; Prescott, Trine; Fagerberg, Christina; Laulund, Lone Walentin; Fregeau, Brieana; Larsen, Martin J; Byler, Melissa; Lebel, Robert Roger; Hurst, Anna C; Dean, Joy; Schrier Vergano, Samantha A; Norman, Jennifer; Mercimek-Andrews, Saadet; Neira, Juanita; Van Allen, Margot I; Wierenga, Klaas J; Longo, Nicola; Sellars, Elizabeth; Louie, Raymond J; Cathey, Sara S; Brokamp, Elly; Heron, Delphine; Snyder, Molly; Vanderver, Adeline; Simon, Celeste; de la Cruz, Xavier; Wadley, Alexandrea; Padilla, Natália; Crump, J Gage; Chung, Wendy; Garcia, Benjamin; Hakonarson, Hakon H; Bhoj, Elizabeth J; Mancini, Grazia M S; Powell-Hamilton, Nina; van de Kamp, Jiddeke; Grebe, Theresa; Dean, John; Ross, Alison; Cox, Samuel G; Crawford, Heather P; Powis, Zoe; Cho, Megan T; Willing, Marcia C; Manwaring, Linda; Schot, Rachel; Nava, Caroline; Afenjar, Alexandra; Lessel, Davor; Wagner, Matias; Marchione, Dylan; Klopstock, Thomas; Winkelmann, Juliane; Catarino, Claudia B; Retterer, Kyle; Schuette, Jane L; Innis, Jeffrey W; Pizzino, Amy; Lüttgen, Sabine; Denecke, Jonas; Strom, Tim M; Joiner, Evan F; Monaghan, Kristin G; Study, DDD; Yuan, Zuo-Fei; Dubbs, Holly; Bend, Renee; Lee, Jennifer A; Lyons, Michael J; Hoefele, Julia; Günthner, Roman; Reutter, Heiko; Wilson, Khadija; Keren, Boris; Radtke, Kelly; Sherbini, Omar; Mrokse, Cameron; Helbig, Katherine L; Odent, Sylvie; Cogne, Benjamin; Mercier, Sandra; Bezieau, Stephane; Besnard, Thomas; Janssen, Kevin; Kury, Sebastien; Redon, Richard; Reinson, Karit; Wojcik, Monica H; Õunap, Katrin; Ilves, Pilvi; Innes, A Micheil; Kernohan, Kristin D; Consortium, Care4Rare Canada; Costain, Gregory; Lee, Pearl; Meyn, M Stephen; Chitayat, David; Zackai, Elaine; Lehman, Anna; Kitson, Hilary; Study, CAUSES; Martin, Martin G; Martinez-Agosto, Julian A; Network, Undiagnosed Diseases; Nelson, Stan F; March, Michael E; Palmer, Christina G S; Papp, Jeanette C; Parker, Neil H; Sinsheimer, Janet S; Vilain, Eric; Wan, Jijun; Yoon, Amanda J; Zheng, Allison; Brimble, Elise; Ferrero, Giovanni Battista; Nair, Divya; Radio, Francesca Clementina; Carli, Diana; Barresi, Sabina; Brusco, Alfredo; Tartaglia, Marco; Thomas, Jennifer Muncy; Umana, Luis; Weiss, Marjan M; Gotway, Garrett; Stuurman, K. E.

Sci Adv
DDD Study, Care4Rare Canada Consortium, CAUSES Study & Undiagnosed Diseases Network 2020, 'Histone H3.3 beyond cancer: Germline mutations in Histone 3 Family 3A and 3B cause a previously unidentified neurodegenerative disorder in 46 patients', Science Advances, vol. 6, no. 49, eabc9207. https://doi.org/10.1126/sciadv.abc9207
Science advances 6(49), eabc9207 (2020). doi:10.1126/sciadv.abc9207
Bryant, L, Li, D, Cox, S G, Marchione, D, Joiner, E F, Wilson, K, Fagerberg, C, Laulund, L W, Larsen, M J & DDD Study 2020, ' Histone H3.3 beyond cancer : Germline mutations in Histone 3 Family 3A and 3B cause a previously unidentified neurodegenerative disorder in 46 patients ', Science Advances, vol. 6, no. 49, eabc9207 . https://doi.org/10.1126/sciadv.abc9207
Science advances, vol 6, iss 49

O’Rawe, Jason A; Wu, Yiyang; Dörfel, Max J; Rope, Alan F; Au, P. Y. Billie; Parboosingh, Jillian S; Moon, Sungjin; Kousi, Maria; Kosma, Konstantina; Smith, Christopher S; Tzetis, Maria; Schuette, Jane L; Hufnagel, Robert B; Prada, Carlos E; Martinez, Francisco; Orellana, Carmen; Crain, Jonathan; Caro-Llopis, Alfonso; Oltra, Silvestre; Monfort, Sandra; Jiménez-Barrón, Laura T; Swensen, Jeffrey; Ellingwood, Sara; Smith, Rosemarie; Fang, Han; Ospina, Sandra; Stegmann, Sander; Den Hollander, Nicolette; Mittelman, David; Highnam, Gareth; Robison, Reid; Yang, Edward; Faivre, Laurence; Roubertie, Agathe; Rivière, Jean-Baptiste; Monaghan, Kristin G; Wang, Kai; Davis, Erica E; Katsanis, Nicholas; Kalscheuer, Vera M; Wang, Edith H; Metcalfe, Kay; Kleefstra, Tjitske; Innes, A. Micheil; Kitsiou-Tzeli, Sophia; Rosello, Monica; Keegan, Catherine E; Lyon, Gholson J

Am J Hum Genet
AMERICAN JOURNAL OF HUMAN GENETICS
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
instname
Instituto de Investigación Sanitaria La Fe (IIS La Fe)
American Journal of Human Genetics, 97, 6, pp. 922-32
The American Journal of Human Genetics
Papai, G., Weil, P.A., Schultz, P., New insights into the function of transcription factor TFIID from recent structural studies (2011) Curr. Opin. Genet. Dev., 21, pp. 219-224
Repositorio EdocUR-U. Rosario
Universidad del Rosario
instacron:Universidad del Rosario

Dixon MW; a University of Michigan Medical School , Ann Arbor , Michigan , USA.; Stem MS; b W.K. Kellogg Eye Center, Department of Ophthalmology and Visual Sciences , University of Michigan , Ann Arbor , Michigan , USA.; Schuette JL; c Department of Pediatrics, Division of Genetics , University of Michigan , Ann Arbor , Michigan , USA.; d Department of Human Genetics , University of Michigan , Ann Arbor , Michigan , USA.; Keegan CE; c Department of Pediatrics, Division of Genetics , University of Michigan , Ann Arbor , Michigan , USA.; d Department of Human Genetics , University of Michigan , Ann Arbor , Michigan , USA.; Besirli CG; b W.K. Kellogg Eye Center, Department of Ophthalmology and Visual Sciences , University of Michigan , Ann Arbor , Michigan , USA.

Publisher: Informa Healthcare Country of Publication: England NLM ID: 9436057 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1744-5094 (Electronic) Linking ISSN: 13816810 NLM ISO Abbreviation: Ophthalmic Genet Subsets: MEDLINE

Sperry ED; Department of Human Genetics, The University of Michigan, Ann Arbor, Michigan.; Department of the Medical Scientist Training Program, The University of Michigan, Ann Arbor, Michigan.; Schuette JL; Department of Human Genetics, The University of Michigan, Ann Arbor, Michigan.; Department of Pediatrics and Communicable Diseases, The University of Michigan, Ann Arbor, Michigan.; van Ravenswaaij-Arts CM; Department of Genetics, University of Groningen, University Medical Centre, Groningen, The Netherlands.; Green GE; Department of Otolaryngology-Head and Neck Surgery, The University of Michigan, Ann Arbor, Michigan.; Martin DM; Department of Human Genetics, The University of Michigan, Ann Arbor, Michigan.; Department of the Medical Scientist Training Program, The University of Michigan, Ann Arbor, Michigan.; Department of Pediatrics and Communicable Diseases, The University of Michigan, Ann Arbor, Michigan.

Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 101235741 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1552-4833 (Electronic) Linking ISSN: 15524825 NLM ISO Abbreviation: Am J Med Genet A Subsets: MEDLINE

Darrat I; Division of Pediatric Otolaryngology, Department of Otolaryngology-Head and Neck Surgery, University of Michigan Health System, Ann Arbor, Michigan.; Bedoyan JK; Chen M; Schuette JL; Lesperance MM

Publisher: John Wiley And Sons Country of Publication: United States NLM ID: 8902541 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1097-0347 (Electronic) Linking ISSN: 10433074 NLM ISO Abbreviation: Head Neck Subsets: MEDLINE

Johnson BV; University of Adelaide and Robinson Research Institute, Adelaide, Australia.; Kumar R; University of Adelaide and Robinson Research Institute, Adelaide, Australia.; Oishi S; School of Biomedical Sciences, The University of Queensland, Brisbane, Australia.; Alexander S; Queensland Brain Institute, The University of Queensland, Brisbane, Australia; Queensland Centre for Mental Health Research, Wacol, Queensland, Australia.; Kasherman M; School of Biomedical Sciences, The University of Queensland, Brisbane, Australia; Griffith Institute for Drug Discovery, Griffith University, Brisbane, Australia.; Vega MS; Queensland Brain Institute, The University of Queensland, Brisbane, Australia.; Ivancevic A; University of Adelaide and Robinson Research Institute, Adelaide, Australia; BioFrontiers Institute, University of Colorado Boulder, Boulder, Colorado.; Gardner A; University of Adelaide and Robinson Research Institute, Adelaide, Australia.; Domingo D; University of Adelaide and Robinson Research Institute, Adelaide, Australia.; Corbett M; University of Adelaide and Robinson Research Institute, Adelaide, Australia.; Parnell E; Department of Physiology, Northwestern University Feinberg School of Medicine, Chicago, Illinois.; Yoon S; Department of Physiology, Northwestern University Feinberg School of Medicine, Chicago, Illinois.; Oh T; Department of Medical Genetics, British Columbia Women's Hospital and University of British Columbia, Vancouver, British Columbia, Canada.; Lines M; Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada.; Lefroy H; Oxford Centre for Genomic Medicine, Oxford University Hospitals National Health Services Foundation Trust, Oxford, United Kingdom.; Kini U; Oxford Centre for Genomic Medicine, Oxford University Hospitals National Health Services Foundation Trust, Oxford, United Kingdom.; Van Allen M; Department of Medical Genetics, University of British Columbia, Vancouver, British Columbia, Canada.; Grønborg S; Center for Rare Diseases, Department of Pediatrics and Department of Clinical Genetics, University Hospital Copenhagen, Copenhagen, Denmark.; Mercier S; Service de Génétique Médicale, Centre Hospitalier Universitaire Nantes and l'Institut du Thorax, Institut National de la Santé et de la Recherche Médicale, Centre National de la Recherche Scientifique, Université de Nantes, Nantes, France.; Küry S; Service de Génétique Médicale, Centre Hospitalier Universitaire Nantes and l'Institut du Thorax, Institut National de la Santé et de la Recherche Médicale, Centre National de la Recherche Scientifique, Université de Nantes, Nantes, France.; Bézieau S; Service de Génétique Médicale, Centre Hospitalier Universitaire Nantes and l'Institut du Thorax, Institut National de la Santé et de la Recherche Médicale, Centre National de la Recherche Scientifique, Université de Nantes, Nantes, France.; Pasquier L; Service de Génétique Clinique, Centre de Référence Déficiences Intellectuelles de Causes Rares, Centre Hospitalier Universitaire Hôpital Sud, Rennes, France.; Raynaud M; Centre Hospitalier Régional Universitaire de Tours, Service de Génétique, Unité Nixte de Recherche 1253, iBrain, Université de Tours, Institut National de la Santé et de la Recherche Médicale, Tours, France.; Afenjar A; Groupe de Recherche Clinique No. 19, ConCer-LD, Département de Génétique, Assistance Publique-Hôpitaux de Paris, Hôpital Armand Trousseau, Centres de Référence Maladies Rares des Déficits Intellectuels de Causes Rares, Paris, France.; Billette de Villemeur T; Sorbonne Université, Groupe de Recherche Clinique No. 19, ConCer-LD, Neuropédiatrie, Centres de Référence Maladies Rares Neurogénétique, Institut National de la Santé et de la Recherche Médicale, Assistance Publique-Hôpitaux de Paris, Hôpital Armand Trousseau, Paris, France.; Keren B; Hôpital de la Pitié-Salpêtrière, Département de Génétique, Paris, France.; Désir J; Erasme University Hospital, Université Libre de Bruxelles, Brussels, Belgium.; Van Maldergem L; Centre de Génétique Humaine, Université de Franche-Comté, Besançon, France.; Marangoni M; Erasme University Hospital, Université Libre de Bruxelles, Brussels, Belgium.; Dikow N; Institute of Human Genetics, Heidelberg University, Heidelberg, Germany.; Koolen DA; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.; VanHasselt PM; Department of Metabolic Diseases, University Medical Center Utrecht, Utrecht, The Netherlands.; Weiss M; Department of Clinical Genetics, Vrije Universiteit University Medical Center, Amsterdam, The Netherlands.; Zwijnenburg P; Medical Genetics Unit, Hospital Pediátrico, Centro Hospitalar e Universitário de Coimbra, Coimbra, Portugal.; Sa J; Medical Genetics Unit, Hospital Pediátrico, Centro Hospitalar e Universitário de Coimbra, Coimbra, Portugal.; Reis CF; Medical Genetics Unit, Hospital Pediátrico, Centro Hospitalar e Universitário de Coimbra, Coimbra, Portugal.; López-Otín C; Departamento de Bioquímica y Biología Molecular, Instituto Universitário de Oncología del Principado de Asturias, Universidad de Oviedo, Oviedo, Spain; Centro de Investigación Biomédica en Red de Cáncer, Spain.; Santiago-Fernández O; Departamento de Bioquímica y Biología Molecular, Instituto Universitário de Oncología del Principado de Asturias, Universidad de Oviedo, Oviedo, Spain.; Fernández-Jaén A; Unidad de Neurología Infantil, Hospital Universitário Quirón Madrid, Madrid, Spain.; Rauch A; Institute of Medical Genetics, University of Zurich, Schlieren, Switzerland.; Steindl K; Institute of Medical Genetics, University of Zurich, Schlieren, Switzerland.; Joset P; Institute of Medical Genetics, University of Zurich, Schlieren, Switzerland.; Goldstein A; Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.; Madan-Khetarpal S; Children's Hospital of Pittsburgh, Pittsburgh, Pennsylvania.; Infante E; Children's Hospital of Pittsburgh, Pittsburgh, Pennsylvania.; Zackai E; Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.; Mcdougall C; Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.; Narayanan V; Center for Rare Childhood Disorders, Translational Genomics Research Institute, Phoenix, Arizona.; Ramsey K; Center for Rare Childhood Disorders, Translational Genomics Research Institute, Phoenix, Arizona.; Mercimek-Andrews S; Division of Clinical and Metabolic Genetics, Department of Pediatrics, University of Toronto, The Hospital for Sick Children, Toronto, Ontario, Canada.; Pena L; Division of Human Genetics, Cincinnati Children's Hospital; Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, Ohio.; Shashi V; Department of Pediatrics, Division of Medical Genetics, Duke University Medical Center, Durham, North Carolina.; Schoch K; Department of Pediatrics, Division of Medical Genetics, Duke University Medical Center, Durham, North Carolina.; Sullivan JA; Department of Pediatrics, Division of Medical Genetics, Duke University Medical Center, Durham, North Carolina.; Pinto E Vairo F; Department of Clinical Genomics, Mayo Clinic, Rochester, Minnesota; Center for Individualized Medicine, Mayo Clinic, Rochester, Minnesota.; Pichurin PN; Department of Clinical Genomics, Mayo Clinic, Rochester, Minnesota.; Ewing SA; Department of Clinical Genomics, Mayo Clinic, Rochester, Minnesota.; Barnett SS; Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota.; Klee EW; Department of Clinical Genomics, Mayo Clinic, Rochester, Minnesota.; Perry MS; Jane and John Justin Neuroscience Center, Cook Children's Medical Center, Fort Worth, Texas.; Koenig MK; Department of Pediatrics, University of Texas Medical School at Houston, Houston, Texas.; Keegan CE; Division of Genetics, Department of Pediatrics, University of Michigan, Ann Arbor, Michigan.; Schuette JL; Division of Genetics, Department of Pediatrics, University of Michigan, Ann Arbor, Michigan.; Asher S; Translational Medicine & Human Genetics, Hospital of the University of Pennsylvania, Philadelphia, Pennsylvania.; Perilla-Young Y; Division of Pediatric Genetics and Metabolism, University of North Carolina, Chapel Hill, North Carolina.; Smith LD; Division of Pediatric Genetics and Metabolism, University of North Carolina, Chapel Hill, North Carolina.; Rosenfeld JA; Baylor College of Medicine, Houston, Texas.; Bhoj E; Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.; Kaplan P; Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.; Li D; Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.; Oegema R; Department of Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.; van Binsbergen E; Department of Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.; van der Zwaag B; Department of Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.; Smeland MF; Department of Medical Genetics, University Hospital of North Norway, Tromsø, Norway.; Cutcutache I; Translational Medicine, UCB Pharma, Slough, United Kingdom.; Page M; Translational Medicine, UCB Pharma, Braine-l'Alleud, Belgium.; Armstrong M; Translational Medicine, UCB Pharma, Braine-l'Alleud, Belgium.; Lin AE; Medical Genetics Unit, Mass General Hospital for Children, Boston, Massachusetts.; Steeves MA; Medical Genetics Unit, Mass General Hospital for Children, Boston, Massachusetts.; Hollander ND; Department of Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands.; Hoffer MJV; Department of Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands.; Reijnders MRF; Department of Clinical Genetics, Maastricht University Medical Center, Maastricht, The Netherlands.; Demirdas S; Department of Clinical Genetics, Erasmus University Medical Center, Rotterdam, The Netherlands.; Koboldt DC; Nationwide Children's Hospital, Columbus, Ohio.; Bartholomew D; Nationwide Children's Hospital, Columbus, Ohio.; Mosher TM; Nationwide Children's Hospital, Columbus, Ohio.; Hickey SE; Department of Pediatrics, The Ohio State University College of Medicine, Columbus, Ohio.; Shieh C; David Geffen School of Medicine, University of California-Los Angeles, California.; Sanchez-Lara PA; Department of Pediatrics, Cedars-Sinai Medical Center, Los Angeles, California.; Graham JM Jr; Department of Pediatrics, Cedars-Sinai Medical Center, Los Angeles, California.; Tezcan K; Department of Genetics, Kaiser Permanente, Sacramento, California.; Schaefer GB; Section of Genetics and Metabolism, University of Arkansas for Medical Sciences, Little Rock, Arkansas.; Danylchuk NR; Department of Genetic Counseling, University of Arkansas for Medical Sciences, Little Rock, Arkansas.; Asamoah A; Department of Pediatrics, University of Louisville School of Medicine, Louisville, Kentucky.; Jackson KE; Department of Pediatrics, University of Louisville School of Medicine, Louisville, Kentucky.; Yachelevich N; Clinical Genetics Services, Department of Pediatrics, New York University School of Medicine, New York, New York.; Au M; Department of Pediatrics, Cedars-Sinai Medical Center, Los Angeles, California.; Pérez-Jurado LA; University of Adelaide and Robinson Research Institute, Adelaide, Australia; Women's and Children's Hospital, Adelaide, Australia; South Australian Health and Medical Research Institute, Adelaide, South Australia; Hospital del Mar Research Institute, Network Research Centre for Rare Diseases and Universitat Pompeu Fabra, Barcelona, Spain.; Kleefstra T; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.; Penzes P; Department of Physiology, Northwestern University Feinberg School of Medicine, Chicago, Illinois.; Wood SA; Griffith Institute for Drug Discovery, Griffith University, Brisbane, Australia.; Burne T; Queensland Brain Institute, The University of Queensland, Brisbane, Australia; Queensland Centre for Mental Health Research, Wacol, Queensland, Australia.; Pierson TM; Department of Pediatrics, Cedars-Sinai Medical Center, Los Angeles, California; Department of Neurology and the Board of Governors Regenerative Medicine Institute, Cedars-Sinai Medical Center, Los Angeles, California.; Piper M; School of Biomedical Sciences, The University of Queensland, Brisbane, Australia; Queensland Brain Institute, The University of Queensland, Brisbane, Australia.; Gécz J; University of Adelaide and Robinson Research Institute, Adelaide, Australia; South Australian Health and Medical Research Institute, Adelaide, South Australia. Electronic address: Jozef.Gecz@adelaide.edu.au.; Jolly LA; University of Adelaide and Robinson Research Institute, Adelaide, Australia. Electronic address: Lachlan.Jolly@adelaide.edu.au.

Publisher: Elsevier Country of Publication: United States NLM ID: 0213264 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1873-2402 (Electronic) Linking ISSN: 00063223 NLM ISO Abbreviation: Biol Psychiatry Subsets: MEDLINE

Waggoner D; Department of Human Genetics, University of Chicago, Chicago, Illinois, USA. dwaggone@genetics.uchicago.edu.; Wain KE; Autism & Developmental Medicine Institute, Geisinger Health System, Danville, Pennsylvania, USA.; Dubuc AM; Department of Pathology, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts, USA.; Conlin L; Department of Pathology and Laboratory Medicine, Perelman School of Medicine, Philadelphia, Pennsylvania, USA.; Hickey SE; Department of Pediatrics, The Ohio State University College of Medicine, Columbus, Ohio, USA.; Lamb AN; Department of Pathology, ARUP Laboratories, University of Utah School of Medicine, Salt Lake City, Utah, USA.; Martin CL; Autism & Developmental Medicine Institute, Geisinger Health System, Danville, Pennsylvania, USA.; Morton CC; Department of Pathology, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts, USA.; Department of Obstetrics and Gynecology and Reproductive Biology, Brigham and Women's Hospital, Broad Institute of MIT and Harvard, Harvard Medical School, Boston, Massachusetts, USA.; Division of Evolution and Genomics Science, School of Biological Sciences, Manchester Academic Health Science Center, Manchester, UK.; Rasmussen K; Department of Medical Genetics, Marshfield Clinic, Marshfield, Wisconsin, USA.; Schuette JL; Department of Human Genetics, University of Michigan School of Medicine, Ann Arbor, Michigan, USA.; Schwartz S; Laboratory Corporation of America® Holdings, Burlington, North Carolina, USA.; Miller DT; Division of Genetics and Genomics, Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts, USA. david.miller2@childrens.harvard.edu.

Publisher: Elsevier Country of Publication: United States NLM ID: 9815831 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1530-0366 (Electronic) Linking ISSN: 10983600 NLM ISO Abbreviation: Genet Med Subsets: MEDLINE

Kiedrowski LA; Department of Cancer Genetics, University of Texas Southwestern Medical Center, 5323 Harry Hines Blvd, Dallas, TX, 75390-9323, USA. lesli.kiedrowski@utsouthwestern.edu.; Department of Human Genetics, University of Michigan, Ann Arbor, Michigan, USA. lesli.kiedrowski@utsouthwestern.edu.; Owens KM; Department of Pediatrics and Communicable Diseases, University of Michigan, Ann Arbor, Michigan, USA.; Yashar BM; Department of Human Genetics, University of Michigan, Ann Arbor, Michigan, USA.; Schuette JL; Department of Pediatrics and Communicable Diseases, University of Michigan, Ann Arbor, Michigan, USA.

Publisher: Wiley Country of Publication: United States NLM ID: 9206865 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1573-3599 (Electronic) Linking ISSN: 10597700 NLM ISO Abbreviation: J Genet Couns Subsets: MEDLINE

Moseley KL; Department of Pediatrics and Communicable Diseases, Child Health Evaluation and Research Unit, Division of General Pediatrics, Mott Children's Hospital, University of Michigan, 300 N. Ingalls St. 6D21, Ann Arbor, MI 48109, USA. klmosele@med.umich.edu; Nasr SZ; Schuette JL; Campbell AD

Publisher: Wiley Country of Publication: United States NLM ID: 9206865 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1573-3599 (Electronic) Linking ISSN: 10597700 NLM ISO Abbreviation: J Genet Couns Subsets: MEDLINE

Bernier FP; Department of Medical Genetics, University of Calgary, Calgary, Alberta, Canada. francois.bernier@albertahealthservices.ca; Caluseriu O; Ng S; Schwartzentruber J; Buckingham KJ; Innes AM; Jabs EW; Innis JW; Schuette JL; Gorski JL; Byers PH; Andelfinger G; Siu V; Lauzon J; Fernandez BA; McMillin M; Scott RH; Racher H; Majewski J; Nickerson DA; Shendure J; Bamshad MJ; Parboosingh JS

Publisher: Cell Press Country of Publication: United States NLM ID: 0370475 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1537-6605 (Electronic) Linking ISSN: 00029297 NLM ISO Abbreviation: Am J Hum Genet Subsets: MEDLINE

Baker DL; Department of Human Genetics, University of Michigan, Ann Arbor, Michigan.; Eash T; Schuette JL; Uhlmann WR

Publisher: Wiley Country of Publication: United States NLM ID: 9206865 Publication Model: Print Cited Medium: Print ISSN: 1059-7700 (Print) Linking ISSN: 10597700 NLM ISO Abbreviation: J Genet Couns Subsets: PubMed not MEDLINE