Your browser doesn't support javascript.
loading
Small posterior fossa in Chiari I malformation affected families is significantly linked to 1q43-44 and 12q23-24.11 using whole exome sequencing.
Musolf, Anthony M; Ho, Winson S C; Long, Kyle A; Zhuang, Zhengping; Argersinger, Davis P; Sun, Haiming; Moiz, Bilal A; Simpson, Claire L; Mendelevich, Elena G; Bogdanov, Enver I; Bailey-Wilson, Joan E; Heiss, John D.
Afiliação
  • Musolf AM; Computational and Statistical Genomics Branch, National Human Genome Research Institute, National Institutes of Health, Baltimore, MD, USA.
  • Ho WSC; Surgical Neurology Branch, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, USA.
  • Long KA; Computational and Statistical Genomics Branch, National Human Genome Research Institute, National Institutes of Health, Baltimore, MD, USA.
  • Zhuang Z; Surgical Neurology Branch, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, USA.
  • Argersinger DP; Neuro-Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
  • Sun H; Surgical Neurology Branch, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, USA.
  • Moiz BA; Computational and Statistical Genomics Branch, National Human Genome Research Institute, National Institutes of Health, Baltimore, MD, USA.
  • Simpson CL; Laboratory of Medical Genetics, Harbin Medical University, Harbin, China.
  • Mendelevich EG; Computational and Statistical Genomics Branch, National Human Genome Research Institute, National Institutes of Health, Baltimore, MD, USA.
  • Bogdanov EI; Computational and Statistical Genomics Branch, National Human Genome Research Institute, National Institutes of Health, Baltimore, MD, USA.
  • Bailey-Wilson JE; Department of Genetics, Genomics, and Informatics, University of Tennessee Health Science Center, Memphis, TN, USA.
  • Heiss JD; Department of Neurology and Rehab, Kazan State Medical University, Kazan, Russia.
Eur J Hum Genet ; 27(10): 1599-1610, 2019 10.
Article em En | MEDLINE | ID: mdl-31227808
Assuntos
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fenótipo / Malformação de Arnold-Chiari / Cromossomos Humanos Par 1 / Cromossomos Humanos Par 12 / Aberrações Cromossômicas / Estudo de Associação Genômica Ampla Tipo de estudo: Prognostic_studies Limite: Female / Humans / Male Idioma: En Revista: Eur J Hum Genet Ano de publicação: 2019 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fenótipo / Malformação de Arnold-Chiari / Cromossomos Humanos Par 1 / Cromossomos Humanos Par 12 / Aberrações Cromossômicas / Estudo de Associação Genômica Ampla Tipo de estudo: Prognostic_studies Limite: Female / Humans / Male Idioma: En Revista: Eur J Hum Genet Ano de publicação: 2019 Tipo de documento: Article