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Article

Fragile X syndrome phenotype with normal FMR1 gene studies.

American journal of medical genetics. Part A - 1 Sept 2004

Clarke Nigel F, Mowat David, Kooy R Frank, Reyniers Edwin, Willemsen Rob

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Source

Identifiers

PMID: 15326639
DOI: 10.1002/ajmg.a.30194

Genes

FMR1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026.

Related research

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Research trail→

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Fragile X syndrome phenotype with normal FMR1 gene studies.PMID 15326639Read ↗

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

ACMG Standards and Guidelines for fragile X testing: a revision to the disease-specific supplements to the Standards and Guidelines for Clinical Genetics Laboratories of the American College of Medical Genetics and Genomics.Semantic proximity Read ↗

Genetic counseling for fragile x syndrome: updated recommendations of the national society of genetic counselors.Semantic proximity Read ↗

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

The fragile-X syndrome after the discovery of the FMR-1 gene. The clinical geneticist faced with the unravelled enigmas and persisting difficulties in genetic counseling.Semantic proximity Read ↗

Molecular and cellular genetics of fragile X syndrome.Semantic proximity Read ↗

Genetic counseling and testing for FMR1 gene mutations: practice guidelines of the national society of genetic counselors.Semantic proximity Read ↗

[Fragile X syndrome: epidemiology, genetics, diagnosis].Semantic proximity Read ↗

Clinical conundrums in fragile X syndrome.Semantic proximity Read ↗

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

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