Fragile X population carrier screening.

Metcalfe, Sylvia A; Delatycki, Martin B; Cohen, Jonathan; Archibald, Alison D; Emery, Jon D

Metcalfe, Sylvia A; Delatycki, Martin B; Cohen, Jonathan; Archibald, Alison D; Emery, Jon D.

Afiliação

Metcalfe SA; Murdoch Childrens Research Institute, Genetics Education and Health Research, Royal Children's Hospital, Melbourne, Victoria, Australia. sylvia.metcalfe@mcri.edu.au.
Delatycki MB; Murdoch Childrens Research Institute, Genetics Education and Health Research, Royal Children's Hospital, Melbourne, Victoria, Australia.
Cohen J; Murdoch Childrens Research Institute, Genetics Education and Health Research, Royal Children's Hospital, Melbourne, Victoria, Australia.
Archibald AD; Murdoch Childrens Research Institute, Genetics Education and Health Research, Royal Children's Hospital, Melbourne, Victoria, Australia.
Emery JD; Murdoch Childrens Research Institute, Genetics Education and Health Research, Royal Children's Hospital, Melbourne, Victoria, Australia.

Genet Med ; 20(9): 1091-1092, 2018 09.

Article em En | MEDLINE | ID: mdl-29215647

Assuntos

Síndrome do Cromossomo X Frágil/genética; Testes Genéticos; Proteína do X Frágil da Deficiência Intelectual; Humanos

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Testes Genéticos / Síndrome do Cromossomo X Frágil Tipo de estudo: Diagnostic_studies / Screening_studies Limite: Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article

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