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Article

Molecular analysis of four males with mental retardation and deletions of Xq21 places the putative MR region in Xq21.1 between DXS233 and CHM.

Human molecular genetics - 1 Aug 1995

May M, Colleaux L, Murgia A, Aylsworth A, Nussbaum R, Fontes M, Schwartz C

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Source

Identifiers

PMID: 7581391
DOI: 10.1093/hmg/4.8.1465

Genes

CHM

Provenance

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

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Research trail→

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Molecular analysis of four males with mental retardation and deletions of Xq21 places the putative MR region in Xq21.1 between DXS233 and CHM.PMID 7581391Read ↗

MRX8: an X-linked mental retardation condition with linkage to Xq21.Semantic proximity Read ↗

Clinical and molecular contributions to the understanding of X-linked mental retardation.Semantic proximity Read ↗

X-linked mental retardation exhibiting linkage to DXS255 and PGKP1: a new MRX family (MRX14) with localization in the pericentromeric region.Semantic proximity Read ↗

Mental retardation in a boy with an interstitial deletion at Xp22.3 involving STS, KAL1, and OA1: implication for the MRX locus.Semantic proximity Read ↗

Syndromic form of X-linked mental retardation with marked hypotonia in early life, severe mental handicap, and difficult adult behavior maps to Xp22.Semantic proximity Read ↗

X-linked mental retardation: vanishing boundaries between non-specific (MRX) and syndromic (MRXS) forms.Semantic proximity Read ↗

A splice site mutation in the methyltransferase gene FTSJ1 in Xp11.23 is associated with non-syndromic mental retardation in a large Belgian family (MRX9).Semantic proximity Read ↗

X-linked mental retardation: a comprehensive molecular screen of 47 candidate genes from a 7.4 Mb interval in Xp11.Semantic proximity Read ↗

A unique form of mental retardation with a distinctive phenotype maps to Xq26-q27.Semantic proximity Read ↗

Stocco dos Santos X-linked mental retardation syndrome: clinical elucidation and localization to Xp11.3-Xq21.3.Semantic proximity Read ↗

Uniparental and functional X disomy in Turner syndrome patients with unexplained mental retardation and X derived marker chromosomes.Semantic proximity Read ↗

X-linked mental retardation: evidence for a recent mutation in a five-generation family (MRX65) linked to the pericentromeric region.Semantic proximity Read ↗

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