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NEXMIF pathogenic variants in individuals of Korean, Vietnamese, and Mexican descent.
Langley, Elizabeth; Farach, Laura S; Koenig, Mary K; Northrup, Hope; Rodriguez-Buritica, David F; Mowrey, Kate.
Afiliação
  • Langley E; Division of Medical Genetics, Department of Pediatrics, McGovern Medical School at the University of Texas Health Science Center at Houston (UTHealth Houston) and Children's Memorial Hermann Hospital, Houston, Texas, USA.
  • Farach LS; Division of Medical Genetics, Department of Pediatrics, McGovern Medical School at the University of Texas Health Science Center at Houston (UTHealth Houston) and Children's Memorial Hermann Hospital, Houston, Texas, USA.
  • Koenig MK; Division of Child and Adolescent Neurology, Department of Pediatrics, McGovern Medical School at the University of Texas Health Science Center at Houston (UTHealth Houston) and Children's Memorial Hermann Hospital, Houston, Texas, USA.
  • Northrup H; Division of Medical Genetics, Department of Pediatrics, McGovern Medical School at the University of Texas Health Science Center at Houston (UTHealth Houston) and Children's Memorial Hermann Hospital, Houston, Texas, USA.
  • Rodriguez-Buritica DF; Division of Medical Genetics, Department of Pediatrics, McGovern Medical School at the University of Texas Health Science Center at Houston (UTHealth Houston) and Children's Memorial Hermann Hospital, Houston, Texas, USA.
  • Mowrey K; Division of Medical Genetics, Department of Pediatrics, McGovern Medical School at the University of Texas Health Science Center at Houston (UTHealth Houston) and Children's Memorial Hermann Hospital, Houston, Texas, USA.
Am J Med Genet A ; 188(6): 1688-1692, 2022 06.
Article em En | MEDLINE | ID: mdl-35146903
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Deficiência Intelectual / Proteínas do Tecido Nervoso Tipo de estudo: Diagnostic_studies Limite: Female / Humans / Male País/Região como assunto: Asia / Mexico Idioma: En Revista: Am J Med Genet A Assunto da revista: GENETICA MEDICA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Deficiência Intelectual / Proteínas do Tecido Nervoso Tipo de estudo: Diagnostic_studies Limite: Female / Humans / Male País/Região como assunto: Asia / Mexico Idioma: En Revista: Am J Med Genet A Assunto da revista: GENETICA MEDICA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos