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A 5-month-old boy with delay in growth and development and decreased muscle tone.
Hucthagowder, Vishwanathan; Shinawi, Marwan; Lockwood, Christina M.
Afiliação
  • Hucthagowder V; Department of Pathology and Immunology, Division of Laboratory Medicine.
  • Shinawi M; Department of Pediatrics, Division of Genetics and Genomic Medicine, Washington University School of Medicine, St. Louis, MO.
  • Lockwood CM; Department of Pathology and Immunology, Division of Laboratory Medicine, clockwood@path.wustl.edu.
Clin Chem ; 61(1): 50-4, 2015 Jan.
Article em En | MEDLINE | ID: mdl-25550475

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de Prader-Willi / Análise Mutacional de DNA / Síndrome de Angelman / Transtornos do Crescimento / Hipotonia Muscular Limite: Humans / Infant / Male Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de Prader-Willi / Análise Mutacional de DNA / Síndrome de Angelman / Transtornos do Crescimento / Hipotonia Muscular Limite: Humans / Infant / Male Idioma: En Ano de publicação: 2015 Tipo de documento: Article