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Article

Screening for fragile X syndrome: information needs for health planners.

Journal of medical screening - 1 Jan 1997

Murray J, Cuckle H, Taylor G, Hewison J

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 9275266
DOI: 10.1177/096914139700400204

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

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Screening for fragile X syndrome: information needs for health planners.PMID 9275266Read ↗

Current controversies in prenatal diagnosis 1: screening for fragile X syndrome.Semantic proximity Read ↗

Research Gaps in Fragile X Syndrome: An Updated Literature Review to Inform Clinical and Public Health Practice.Semantic proximity Read ↗

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

Genetic epidemiology of the fragile X syndrome with special reference to genetic counseling.Semantic proximity Read ↗

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

ACOG committee opinion. No. 338: Screening for fragile X syndrome.Semantic proximity Read ↗

Population based prenatal screening for the fragile X syndrome.Semantic proximity Read ↗

Diagnosis and management of fragile X syndrome.Semantic proximity Read ↗

[Fragile X syndrome: a review of diagnosis and treatment].Semantic proximity Read ↗

The fragile X-associated disorders: time to order fragile X DNA testing.Semantic proximity Read ↗

Prevalence of fragile X syndrome.Semantic proximity Read ↗

Diagnosing fragile X syndrome.Semantic proximity Read ↗

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