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Ethnicity has a multiplex impact upon the risk of a full mutation expansion among female heterozygotes for FMR1 premutation.
Domniz, Noam; Levavi, Liat Ries; Berkenstadt, Michal; Pras, Elon; Cohen, Yoram; Raanani, Hila; Goldstein, Dana Brabbing; Yaron, Yuval; Elizur, Shai; Ben-Shachar, Shay.
Afiliação
  • Domniz N; IVF Unit, Sheba Medical Center Tel Hashomer, Ramat Gan, Israel.
  • Levavi LR; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
  • Berkenstadt M; The Genetic Institute, Sheba Medical Center Tel Hashomer, Ramat Gan, Israel.
  • Pras E; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
  • Cohen Y; The Genetic Institute, Sheba Medical Center Tel Hashomer, Ramat Gan, Israel.
  • Raanani H; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
  • Goldstein DB; The Genetic Institute, Sheba Medical Center Tel Hashomer, Ramat Gan, Israel.
  • Yaron Y; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
  • Elizur S; IVF Unit, Sheba Medical Center Tel Hashomer, Ramat Gan, Israel.
  • Ben-Shachar S; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
Genet Med ; 23(6): 1023-1027, 2021 06.
Article em En | MEDLINE | ID: mdl-33473206
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteína do X Frágil da Deficiência Intelectual / Síndrome do Cromossomo X Frágil Tipo de estudo: Diagnostic_studies / Etiology_studies / Risk_factors_studies Limite: Female / Humans País como assunto: Asia Idioma: En Ano de publicação: 2021 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteína do X Frágil da Deficiência Intelectual / Síndrome do Cromossomo X Frágil Tipo de estudo: Diagnostic_studies / Etiology_studies / Risk_factors_studies Limite: Female / Humans País como assunto: Asia Idioma: En Ano de publicação: 2021 Tipo de documento: Article