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Article

[Phenotypic screening for X-linked mental retardation: fragile Xq syndrome].

Revista chilena de pediatria - 1 Jan 2000

Lacassie I, Zavala A B, Curotto B, Alliende M A, De Andraca I

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Identifiers

PMID: 7182864

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

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[Phenotypic screening for X-linked mental retardation: fragile Xq syndrome].PMID 7182864Read ↗

[Clinical and genetic aspects of fragile X mental retardation syndrome].Semantic proximity Read ↗

[X-linked mental retardation syndromes].Semantic proximity Read ↗

[X-linked mental retardation: a continuous spectrum from syndromic forms towards non-specific forms].Semantic proximity Read ↗

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

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

[Fragile X syndrome and mental disorders].Semantic proximity Read ↗

[Fragile X syndrome].Semantic proximity Read ↗

[Fragile X syndrome].Semantic proximity Read ↗

[Martin-Bell syndrome (mental retardation with fragile X syndrome (review of the literature)].Semantic proximity Read ↗

[Current aspects in the diagnosis of fragile X syndrome].Semantic proximity Read ↗

[Mental retardation linked to the fragile X. Still questions...].Semantic proximity Read ↗

[A familial case of mental retardation syndrome linked to fragile X chromosome].Semantic proximity Read ↗

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