Bain type of X-linked syndromic mental retardation in boys.

Harmsen, Stefani; Buchert, Rebecca; Mayatepek, Ertan; Haack, Tobias B; Distelmaier, Felix

Harmsen, Stefani; Buchert, Rebecca; Mayatepek, Ertan; Haack, Tobias B; Distelmaier, Felix.

Afiliação

Harmsen S; Department of General Pediatrics, Neonatology and Pediatric Cardiology, University Children's Hospital Duesseldorf, Medical Faculty, Heinrich Heine University, Duesseldorf, Germany.
Buchert R; Institute of Medical Genetics and Applied Genomics, University of Tuebingen, Tuebingen, Germany.
Mayatepek E; Centre for Rare Diseases, University of Tuebingen, Tuebingen, Germany.
Haack TB; Department of General Pediatrics, Neonatology and Pediatric Cardiology, University Children's Hospital Duesseldorf, Medical Faculty, Heinrich Heine University, Duesseldorf, Germany.
Distelmaier F; Institute of Medical Genetics and Applied Genomics, University of Tuebingen, Tuebingen, Germany.

Clin Genet ; 95(6): 734-735, 2019 06.

Article em En | MEDLINE | ID: mdl-30887513

Assuntos

Deficiência Intelectual; Deficiência Intelectual Ligada ao Cromossomo X; Humanos; Masculino; Síndrome

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Deficiência Intelectual Ligada ao Cromossomo X / Deficiência Intelectual Limite: Humans / Male Idioma: En Revista: Clin Genet Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Alemanha País de publicação: Dinamarca

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