Molecular Screening of FRAXA and FRAXE in Indian Patients with Unexplained Mental Retardation
Author:
Affiliation:
1. Department of Medical Genetics, Sanjay Gandhi Post Graduate Institute of Medical Sciences, Lucknow, Uttar Pradesh 226014, India.
Publisher
Mary Ann Liebert Inc
Subject
Genetics (clinical)
Link
http://www.liebertpub.com/doi/pdf/10.1089/10906570260471903
Reference32 articles.
1. Prevalence and Phenotype Consequence of FRAXA and FRAXE Alleles in a Large, Ethnically Diverse, Special Education–Needs Population
2. Fragile X syndrome among children with mental retardation
3. Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox
4. Evaluation of school children at high risk for fragile X syndrome utilizing buccal cell FMR-1 testing
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