Fragile X syndrome: Diagnostic and carrier testing
- 1 October 2005
- journal article
- Published by Elsevier in Genetics in Medicine
- Vol. 7 (8) , 584-587
- https://doi.org/10.1097/01.gim.0000182468.22666.dd
Abstract
No abstract availableKeywords
This publication has 17 references indexed in Scilit:
- Paternal transmission of fragile X syndromeAmerican Journal of Medical Genetics Part A, 2004
- Fragile X Premutation Tremor/Ataxia Syndrome: Molecular, Clinical, and Neuroimaging CorrelatesAmerican Journal of Human Genetics, 2003
- Expansion of the Fragile X CGG Repeat in Females with Premutation or Intermediate AllelesAmerican Journal of Human Genetics, 2003
- Paternally Transmitted FMR1 Alleles Are Less Stable than Maternally Transmitted Alleles in the Common and Intermediate Size RangeAmerican Journal of Human Genetics, 2002
- Prevalence of the fragile X syndrome in African‐AmericansAmerican Journal of Medical Genetics, 2002
- FMR1 and the fragile X syndrome: Human genome epidemiology reviewGenetics in Medicine, 2001
- Prevalence and Phenotype Consequence of FRAXA and FRAXE Alleles in a Large, Ethnically Diverse, Special Education–Needs PopulationAmerican Journal of Human Genetics, 1999
- FMR1 Protein: Conserved RNP Family Domains and Selective RNA BindingScience, 1993
- Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradoxCell, 1991
- Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndromePublished by Elsevier ,1991