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J-GLOBAL ID：201002223048570196   Reference number：10A0545534

Consensus Statement: Chromosomal Microarray Is a First-Tier Clinical Diagnostic Test for Individuals with Developmental Disabilities or Congenital Anomalies

コンセンサス記述 染色体のマイクロアレイは発達障害または先天奇形による個体のための第一段臨床診断検査である

Author (33)： MILLER David T. (Div. of Genetics and Dep. of Lab. Medicine, Children’s Hospital Boston and Harvard Medical School, Boston, MA, USA) ,  ADAM Margaret P. (Dep. of Human Genetics, Emory Univ. School of Medicine, Atlanta, GA, USA) ,  ADAM Margaret P. (Dep. of Pediatrics, Univ. of Washington School of Medicine, Seattle, WA, USA) ,  ARADHYA Swaroop (GeneDx, Gaithersburg, MD, USA) ,  BIESECKER Leslie G. (National Human Genome Res. Inst., National Institutes of Health, Bethesda, MD, USA) ,  BROTHMAN Arthur R. (Dep. of Pediatrics, Human Genetics, Pathology and ARUP Laboratories, Univ. of Utah School of Medicine, Salt Lake ...) ,  CARTER Nigel P. (Wellcome Trust Sanger Inst., Cambridge, UK, USA) ,  CHURCH Deanna M. (National Center for Biotechnology Information, Bethesda, MD, USA) ,  CROLLA John A. (National Genetics Reference Lab. (Wessex), Salisbury UK) ,  EICHLER Evan E. (Dep. of Genome Sciences and Howard Hughes Medical Inst., Univ. of Washington School of Medicine, Seattle, WA, USA) ,  EPSTEIN Charles J. (Inst. for Human Genetics and Dep. of Pediatrics, Univ. of California, San Francisco, San Francisco, CA, USA) ,  FAUCETT W. Andrew (Dep. of Human Genetics, Emory Univ. School of Medicine, Atlanta, GA, USA) ,  FEUK Lars (Rudbeck Lab., Uppsala Univ., Uppsala, SWE) ,  FRIEDMAN Jan M. (Dep. of Medical Genetics, Univ. of British Columbia, and Child & Family Res. Inst., Vancouver, British Columbia, CAN) ,  HAMOSH Ada (Dep. of Pediatrics and McKusick-Nathans Inst. of Genetic Medicine, Johns Hopkins Univ. School of Medicine, Baltimore ...) ,  JACKSON Laird (Dep. of Obstetrics and Gynecology, Drexel Univ. Coll. of Medicine and Children’s Hospital of Philadelphia ...) ,  KAMINSKY Erin B. (Dep. of Human Genetics, Emory Univ. School of Medicine, Atlanta, GA, USA) ,  KOK Klaas (Dep. of Genetics, Univ. Medical Centre Groningen, Univ. of Groningen, NLD) ,  KRANTZ Ian D. (Dep. of Pediatrics/Human Genetics, The Children’s Hospital of Philadelphia, Univ. of Pennsylvania School of Medicine ...) ,  KUHN Robert M. (Center for Biomolecular Sci. and Engineering, Univ. of California, Santa Cruz, Santa Cruz, CA, USA) ,  LEE Charles (Dep. of Pathology, Brigham and Women’s Hospital, Harvard Medical School, Boston, MA, USA) ,  OSTELL James M. (National Center for Biotechnology Information, Bethesda, MD, USA) ,  ROSENBERG Carla (Dep. of Genetics and Evolutionary Biology, Univ. Sao Paulo, BRA) ,  SCHERER Stephen W. ,  SPINNER Nancy B. (Dep. of Pediatrics/Human Genetics, The Children’s Hospital of Philadelphia, Univ. of Pennsylvania School of Medicine ...) ,  STAVROPOULOS Dimitri J. ,  TEPPERBERG James H. ,  THORLAND Erik C. ,  VERMEESCH Joris R. ,  WAGGONER Darrel J. ,  WATSON Michael S. ,  MARTIN Christa Lese (Dep. of Human Genetics, Emory Univ. School of Medicine, Atlanta, GA, USA) ,  LEDBETTER David H. (Dep. of Human Genetics, Emory Univ. School of Medicine, Atlanta, GA, USA)
Material： American Journal of Human Genetics  (AJHG)
Volume： 86  Issue： 5  Page： 749-764  Publication year： May. 14, 2010 
JST Material Number： B0360B  ISSN： 0002-9297  Document type： Article
Country of issue： Netherlands (NLD)  Language： ENGLISH (EN)

Terms in the title (9)： コンセンサス ,  記述 ,  染色体 ,  マイクロアレイ ,  発達障害 ,  先天奇形 ,  個体 ,  臨床 ,  診断検査