The risk of fragile X premutation expansion is lower in carriers detected by general prenatal screening  than in carriers from known fragile X families.

Geva, E; Yaron, Y; Shomrat, R; Ben-Yehuda, A; Zabari, S; Peretz, H; Naiman, T; Yeger, H; Orr-Urtreger, A

The risk of fragile X premutation expansion is lower in carriers detected by general prenatal screening than in carriers from known fragile X families.

Geva, E; Yaron, Y; Shomrat, R; Ben-Yehuda, A; Zabari, S; Peretz, H; Naiman, T; Yeger, H; Orr-Urtreger, A.

Affiliation

Geva E; Department of Obstetrics and Gynecology, Tel Aviv Sourasky Medical Center, Israel.

Genet Test ; 4(3): 289-92, 2000.

Article de En | MEDLINE | ID: mdl-11142761

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Collection: 01-internacional Base de données: MEDLINE Sujet principal: Dépistage génétique / Protéines de liaison à l'ARN / Syndrome du chromosome X fragile / Dépistage des porteurs génétiques / Mutation / Protéines de tissu nerveux Type d'étude: Diagnostic_studies / Etiology_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Limites: Female / Humans / Pregnancy Langue: En Journal: Genet Test Sujet du journal: GENETICA Année: 2000 Type de document: Article Pays d'affiliation: Israël Pays de publication: États-Unis d'Amérique

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