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Article

CGG repeat expansion at FMR1 locus - A new molecular diagnostic algorithm in fragile X syndrome.

Neurology India - 1 Jan 2000

Kumar Neeraj, Malhotra Hardeep Singh, Garg Ravindra Kumar

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Identifiers

PMID: 27841172
DOI: 10.4103/0028-3886.193771

Genes

FMR1

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Related research

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CGG repeat expansion at FMR1 locus - A new molecular diagnostic algorithm in fragile X syndrome.PMID 27841172Read ↗

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Re-examination of factors associated with expansion of CGG repeats using a single nucleotide polymorphism in FMR1.Semantic proximity Read ↗

Beyond Trinucleotide Repeat Expansion in Fragile X Syndrome: Rare Coding and Noncoding Variants in FMR1 and Associated Phenotypes.Semantic proximity Read ↗

Reduction in the number of CGG repeats on the FMR1 gene in carriers of genetic disorders versus noncarriers.Semantic proximity Read ↗

Mechanisms of the FMR1 Repeat Instability: How Does the CGG Sequence Expand?Semantic proximity Read ↗

FMR1 and the fragile X syndrome: human genome epidemiology review.Semantic proximity Read ↗

[Fragile X syndrome and FMR1-dependent diseases - clinical presentation, epidemiology and molecular background].Semantic proximity Read ↗

Intragenic FMR1 disease-causing variants: a significant mutational mechanism leading to Fragile-X syndrome.Semantic proximity Read ↗

Clinical aspects of the fragile X syndrome.Semantic proximity Read ↗

[Fragile X syndrome and FMR1-dependent diseases - diagnostic scheme based on own experience .]Semantic proximity Read ↗

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