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Rare copy number variation in cerebral palsy.
McMichael, Gai; Girirajan, Santhosh; Moreno-De-Luca, Andres; Gecz, Jozef; Shard, Chloe; Nguyen, Lam Son; Nicholl, Jillian; Gibson, Catherine; Haan, Eric; Eichler, Evan; Martin, Christa Lese; MacLennan, Alastair.
Afiliação
  • McMichael G; Robinson Institute, The University of Adelaide, Adelaide, South Australia, Australia.
  • Girirajan S; Department of Genome Sciences, University of Washington School of Medicine, Seattle, WA, USA.
  • Moreno-De-Luca A; Autism and Developmental Medicine Institute, Genomic Medicine Institute, and Department of Pediatrics, Geisinger Health System, Danville, PA, USA.
  • Gecz J; 1] Genetics and Molecular Pathology, SA Pathology at Women's and Children's Hospital, Adelaide, Australia [2] Department of Paediatrics at the Women's and Children's Hospital, The University of Adelaide, Adelaide, South Australia, Australia.
  • Shard C; Department of Paediatrics at the Women's and Children's Hospital, The University of Adelaide, Adelaide, South Australia, Australia.
  • Nguyen LS; Department of Paediatrics at the Women's and Children's Hospital, The University of Adelaide, Adelaide, South Australia, Australia.
  • Nicholl J; Genetics and Molecular Pathology, SA Pathology at Women's and Children's Hospital, Adelaide, Australia.
  • Gibson C; Robinson Institute, The University of Adelaide, Adelaide, South Australia, Australia.
  • Haan E; South Australian Clinical Genetics Service, SA Pathology at Women's and Children's Hospital, and Discipline of Paediatrics, The University of Adelaide, Adelaide, South Australia, Australia.
  • Eichler E; Department of Genome Sciences, University of Washington School of Medicine, Seattle, WA, USA.
  • Martin CL; Department of Human Genetics, Emory University School of Medicine, Atlanta, GA, USA.
  • MacLennan A; Robinson Institute, The University of Adelaide, Adelaide, South Australia, Australia.
Eur J Hum Genet ; 22(1): 40-5, 2014 Jan.
Article em En | MEDLINE | ID: mdl-23695280
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Paralisia Cerebral / Análise em Microsséries / Variações do Número de Cópias de DNA Tipo de estudo: Etiology_studies Limite: Adult / Female / Humans / Infant / Male / Newborn Idioma: En Ano de publicação: 2014 Tipo de documento: Article
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Paralisia Cerebral / Análise em Microsséries / Variações do Número de Cópias de DNA Tipo de estudo: Etiology_studies Limite: Adult / Female / Humans / Infant / Male / Newborn Idioma: En Ano de publicação: 2014 Tipo de documento: Article