X-linked intellectual disability: Phenotypic expression in carrier females.

Ziats, Catherine A; Schwartz, Charles E; Gecz, Jozef; Shaw, Marie; Field, Michael J; Stevenson, Roger E; Neri, Giovanni

Ziats, Catherine A; Schwartz, Charles E; Gecz, Jozef; Shaw, Marie; Field, Michael J; Stevenson, Roger E; Neri, Giovanni.

Afiliação

Ziats CA; J.C. Self Research Institute of Human Genetics, Greenwood Genetic Center, Greenwood, South Carolina.
Schwartz CE; J.C. Self Research Institute of Human Genetics, Greenwood Genetic Center, Greenwood, South Carolina.
Gecz J; Adelaide Medical School, Faculty of Health and Medical Sciences, The University of Adelaide, Adelaide, South Australia, Australia.
Shaw M; Robinson Research Institute, The University of Adelaide, Adelaide, South Australia, Australia.
Field MJ; Women and Kids, South Australian Health and Medical Research Institute, Adelaide, South Australia, Australia.
Stevenson RE; Adelaide Medical School, Faculty of Health and Medical Sciences, The University of Adelaide, Adelaide, South Australia, Australia.
Neri G; Hunter Genetics, Waratah, New South Wales, Australia.

Clin Genet ; 97(3): 418-425, 2020 03.

Article em En | MEDLINE | ID: mdl-31705537

Assuntos

Deficiência Intelectual/genética; Feminino; Genes Ligados ao Cromossomo X/genética; Heterozigoto; Humanos; Fenótipo; Inativação do Cromossomo X

Palavras-chave

X-inactivation; X-linkage; female carriers; intellectual disability

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Deficiência Intelectual Limite: Female / Humans Idioma: En Revista: Clin Genet Ano de publicação: 2020 Tipo de documento: Article País de publicação: Dinamarca

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