부산대학교 도서관

Huang L; The Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, Ontario, Canada.; Vanstone MR; The Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, Ontario, Canada.; Hartley T; The Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, Ontario, Canada.; Osmond M; The Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, Ontario, Canada.; Barrowman N; The Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, Ontario, Canada.; Department of Pediatrics, University of Ottawa, Ottawa, Ontario, Canada.; Allanson J; Department of Pediatrics, University of Ottawa, Ottawa, Ontario, Canada.; Department of Genetics, The Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada.; Baker L; Division of Medical Genetics, A. 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Litwin Family Centre in Genetic Medicine, University Health Network and Mount Sinai Hospital, University of Toronto, Toronto, Ontario, Canada.; Favaro FP; Department of Clinical Genetics, Hospital for Rehabilitation of Craniofacial Anomalies, University of São Paulo, Bauru, Brazil.; Goel H; Hunter Genetics, Newcastle, Waratah, Australia.; University of Newcastle, Newcastle - School of Medicine and Public Health, Faculty of Health, Callaghan, Australia.; Gregersen PA; Department of Clinical Genetics, Aarhus University Hospital, Aarhus, Denmark.; Gripp KW; Division of Medical Genetics, A. I. duPont Hospital for Children, Wilmington, Delaware.; Grix A; Department of Genetics, Permanente Medical Group, Roseville, California.; Guion-Almeida ML; Department of Clinical Genetics, Hospital for Rehabilitation of Craniofacial Anomalies, University of São Paulo, Bauru, Brazil.; Harr MH; Division of Human Genetics, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.; The Perelman School of Medicine of the University of Pennsylvania, Philadelphia, Pennsylvania.; Hudson C; Shodair Children's Hospital, Helena, Montana.; Hunter AG; Medical Geneticist, Ottawa, Ontario, Canada.; Johnson J; Shodair Children's Hospital, Helena, Montana.; Clinical Genetics and Metabolism, Floating Hospital for Children, Tufts Medical Center, Boston, Massachusetts.; Joss SK; West of Scotland Clinical Genetics Service, South Glasgow University Hospital, Glasgow, UK.; Kimball A; Harvey Institute for Human Genetics, Greater Baltimore Medical Center, Baltimore, Maryland.; Kini U; Department of Clinical Genetics, Oxford University Hospitals NHS Trust, Oxford, UK.; Kline AD; Harvey Institute for Human Genetics, Greater Baltimore Medical Center, Baltimore, Maryland.; Lauzon J; Department of Medical Genetics, Alberta Children's Hospital Research Institute, University of Calgary, Calgary, Alberta, Canada.; Lildballe DL; Department of Clinical Genetics, Aarhus University Hospital, Aarhus, Denmark.; López-González V; Sección de Genética Médica, Servicio de Pediatría, Hospital Clínico Universitario Virgen de la Arrixaca, IMIB-Arrixaca, Murcia, Spain.; Grupo Clínico Vinculado al Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Instituto de Salud Carlos III (ISCIII), Madrid, Spain.; Martinezmoles J; Department of Genetics, Sacramento Medical Center, Sacramento, California.; Meldrum C; NSW Health Pathology, Newcastle, Australia.; Mirzaa GM; Division of Genetic Medicine, Department of Pediatrics, University of Washington, Seattle, Washington.; Center for Integrative Brain Research, Seattle Children's Research Institute, Seattle, Washington.; Morel CF; The Fred A. Litwin Family Centre in Genetic Medicine, University Health Network and Mount Sinai Hospital, University of Toronto, Toronto, Ontario, Canada.; Morton JE; West Midlands Regional Genetics Service, Birmingham Women's Hospital, Birmingham, UK.; Pyle LC; Department of Pediatrics, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania.; Quintero-Rivera F; Department of Pathology and Laboratory Medicine, UCLA Clinical Genomics Center, David Geffen School of Medicine, University of California, Los Angeles, California.; Richer J; The Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, Ontario, Canada.; Department of Genetics, The Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada.; Scheuerle AE; Department of Pediatrics, University of Texas Southwestern Medical Center, Dallas, Texas.; Schönewolf-Greulich B; Genetic Counselling Clinic Kennedy Center, Copenhagen University Hospital, Rigshospitalet, Glostrup, Denmark.; Shears DJ; Oxford Regional Genetics Service, The Churchill Hospital, Oxford University Hospitals NHS Trust, Oxford, UK.; Silver J; The Fred A. Litwin Family Centre in Genetic Medicine, University Health Network and Mount Sinai Hospital, University of Toronto, Toronto, Ontario, Canada.; Smith AC; Department of Genetics, The Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada.; Temple IK; Human Development and Health, Faculty of Medicine, University of Southampton, Southampton, UK.; Wessex Clinical Genetics Service, Princess Anne Hospital, University Hospital Southampton NHS Foundation Trust, Southampton, UK.; van de Kamp JM; Department of Clinical Genetics, VU Medical Center, Amsterdam, The Netherlands.; van Dijk FS; Department of Clinical Genetics, VU Medical Center, Amsterdam, The Netherlands.; Vandersteen AM; Maritime Medical Genetics Service, IWKHealth Centre, Halifax, Nova Scotia, Canada.; White SM; Victoria Clinical Genetics Service, Murdoch Children's Research Institute, Melbourne, Australia.; Department of Paediatrics, University of Melbourne, Melbourne, Australia.; Zackai EH; Division of Human Genetics, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.; Department of Pediatrics, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania.; Zou R; The Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, Ontario, Canada.; Bulman DE; The Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, Ontario, Canada.; Newborn Screening Ontario, The Children's Hospital of Eastern Ontario, Ottawa, Canada.; Boycott KM; The Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, Ontario, Canada.; Department of Genetics, The Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada.; Lines MA; The Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, Ontario, Canada.; Department of Pediatrics, University of Ottawa, Ottawa, Ontario, Canada.; Metabolics and Newborn Screening, Department of Pediatrics, The Children's Hospital of Eastern Ontario, Ottawa, Canada.

Publisher: Wiley-Liss Country of Publication: United States NLM ID: 9215429 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1098-1004 (Electronic) Linking ISSN: 10597794 NLM ISO Abbreviation: Hum Mutat Subsets: MEDLINE

Negraes PD; Favaro FP; Camargo JL; Oliveira ML; Goldberg J; Rainho CA; Salvadori DM; Negraes, Priscilla D; Favaro, Francine P; Camargo, João Lauro V; Oliveira, Maria Luiza C S; Goldberg, José; Rainho, Cláudia A; Salvadori, Daisy M F

BMC Cancer. 2008, Vol. 8, p238-238. 1p.

Favaro FP; Departamento de Genética Clínica, Hospital de Reabilitação de Anomalias Craniofaciais, Universidade de São Paulo (HRAC-USP), 17012-090, Bauru, São Paulo, Brasil.; Alvizi L; Centro de Estudos do Genoma Humano, Instituto de Biociências, Universidade de São Paulo, 05508-090, São Paulo, São Paulo, Brasil.; Zechi-Ceide RM; Departamento de Genética Clínica, Hospital de Reabilitação de Anomalias Craniofaciais, Universidade de São Paulo (HRAC-USP), 17012-090, Bauru, São Paulo, Brasil.; Bertola D; Centro de Estudos do Genoma Humano, Instituto de Biociências, Universidade de São Paulo, 05508-090, São Paulo, São Paulo, Brasil.; Felix TM; Hospital das Clínicas de Porto Alegre, Departamento de Genética, Universidade Federal do Rio Grande do Sul, 90035-903, Porto Alegre, Rio Grande do Sul, Brasil.; de Souza J; Centro de Atendimento Integral ao Fissurado Lábio Palatal, 80150-000, Curitiba, Paraná, Brasil.; Raskin S; Núcleo de Investigação Molecular Avançada, Centro de Ciências Biológicas e da Saúde, Pontifícia Universidade Católica do Paraná, 80150-000, Curitiba, Paraná, Brasil.; Twigg SR; Clinical Genetics Group, Weatherall Institute of Molecular Medicine, University of Oxford, Oxford OX3 9DS, UK.; Weiner AM; Instituto de Biología Molecular y Celular de Rosario (IBR), Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET) - Facultad de Ciencias Bioquímicas y Farmacéuticas, Universidad Nacional de Rosario, S2000FHQ, Rosario, Argentina.; Armas P; Instituto de Biología Molecular y Celular de Rosario (IBR), Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET) - Facultad de Ciencias Bioquímicas y Farmacéuticas, Universidad Nacional de Rosario, S2000FHQ, Rosario, Argentina.; Margarit E; Instituto de Biología Molecular y Celular de Rosario (IBR), Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET) - Facultad de Ciencias Bioquímicas y Farmacéuticas, Universidad Nacional de Rosario, S2000FHQ, Rosario, Argentina.; Calcaterra NB; Instituto de Biología Molecular y Celular de Rosario (IBR), Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET) - Facultad de Ciencias Bioquímicas y Farmacéuticas, Universidad Nacional de Rosario, S2000FHQ, Rosario, Argentina.; Andersen GR; Department of Molecular Biology and Genetics. Aarhus University, Gustav Wieds Vej 10C, 8000 Aarhus, Denmark.; McGowan SJ; Computational Biology Research Group, Weatherall Institute of Molecular Medicine, University of Oxford, Oxford OX3 9DS, UK.; Wilkie AO; Clinical Genetics Group, Weatherall Institute of Molecular Medicine, University of Oxford, Oxford OX3 9DS, UK.; Richieri-Costa A; Departamento de Genética Clínica, Hospital de Reabilitação de Anomalias Craniofaciais, Universidade de São Paulo (HRAC-USP), 17012-090, Bauru, São Paulo, Brasil.; de Almeida ML; Departamento de Genética Clínica, Hospital de Reabilitação de Anomalias Craniofaciais, Universidade de São Paulo (HRAC-USP), 17012-090, Bauru, São Paulo, Brasil.; Passos-Bueno MR; Centro de Estudos do Genoma Humano, Instituto de Biociências, Universidade de São Paulo, 05508-090, São Paulo, São Paulo, Brasil. Electronic address: passos@ib.usp.br.

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

Favaro FP; Department of Clinical Genetics, Hospital of Rehabilitation of Craniofacial Anomalies, University of São Paulo (HRAC-USP), Bauru, SP, Brazil.; Zechi-Ceide RM; Alvarez CW; Maximino LP; Antunes LF; Richieri-Costa A; Guion-Almeida ML

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