Fully mutated and gray-zoneFRAXA alleles in Brazilian mentally retarded boys
- 29 April 1999
- journal article
- Published by Wiley in American Journal of Medical Genetics
- Vol. 84 (3) , 198-201
- https://doi.org/10.1002/(sici)1096-8628(19990528)84:3<198::aid-ajmg5>3.0.co;2-w
Abstract
No abstract availableKeywords
This publication has 15 references indexed in Scilit:
- Simultaneous detection of size and sequence polymorphisms in the transcribed trinucleotide repeat D2S196E (EST00493)Human Genetics, 1997
- A PCR-based test suitable for screening for fragile X syndrome among mentally retarded malesHuman Genetics, 1996
- Population screening at the FRAXA and FRAXE loci: molecular analyses of boys with learning difficulties and their mothersHuman Molecular Genetics, 1996
- An n-allele model for progressive amplification in the FMR1 locus.Proceedings of the National Academy of Sciences, 1995
- Evaluation of school children at high risk for fragile X syndrome utilizing buccal cell FMR‐1 testingAmerican Journal of Medical Genetics, 1994
- Relationship of expansion of CGG repeats and X-inactivation with expression of fra(X) (q27.3) in heterozygotesAmerican Journal of Medical Genetics, 1994
- CAT repeat polymorphism in a human expressed sequence tag (EST00444) (D1 3S308)Human Molecular Genetics, 1993
- Population studies of the fragile X: a molecular approach.Journal of Medical Genetics, 1993
- Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradoxCell, 1991
- Fragile X frequency in a mentally retarded population in BrazilAmerican Journal of Medical Genetics, 1990