Fragile X syndrome: examination of issues pertaining to population-based screening
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology and Child Health
Reference77 articles.
1. Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome;Verkerk;Cell,1991
2. Variation of the CGG repeat at the fragile X site results in genetic instability: resolution of the Sherman paradox;Fu;Cell,1991
3. Fragile X genotype characterized by an unstable region of DNA;Yu;Science,1991
4. Length of uninterrupted CGG repeats determines instability in the FMR1 gene;Eichler;Nature Genet,1994
5. Cryptic and polar variation of the fragile X repeat could result in predisposing normal alleles;Kunst;Cell,1994
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1. Carrier screening in preconception consultation in primary care;Journal of Community Genetics;2011-12-20
2. A model for offering carrier screening for fragile X syndrome to nonpregnant women: results from a pilot study;Genetics in Medicine;2008-07
3. ABAS-II;Adaptive Behavior Assessment System-II;2008
4. Screening for fragile X syndrome: results from a school for mentally retarded children;Acta Paediatrica;2007-01-02
5. Women’s Attitudes Toward Testing for Fragile X Carrier Status: A Qualitative Analysis;Journal of Genetic Counseling;2005-08
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