Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Familial X-linked mental retardation and isolated growth hormone deficiency: Clinical and molecular findings

12 Jul 1996

Abstract excerpt

We report on several members of a family with varying degrees of X-linked mental retardation (XLMR), isolated growth hormone deficiency (IGHD), and infantile behaviour but without other consistent phenotypic abnormalities. Male patients continued to grow until well into their twenties and reached a height ranging from 135 to 159 cm. Except one, all female carriers were mentally normal; their adult height ranged...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Genetics and Neurodevelopmental Disorders
Share to Growth Hormone and Insulin-like Growth Factors
Share to RNA modifications and cancer

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Source

Identifiers

PMID: 8826446
DOI: 10.1002/(sici)1096-8628(19960712)64:1<35::aid-ajmg5>3.0.co;2-q

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

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

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Familial X-linked mental retardation and isolated growth hormone deficiency: Clinical and molecular findingsPMID 8826446Read ↗

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

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

X-linked mental retardation: further lumping, splitting and emerging phenotypes.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].Semantic proximity Read ↗

XLMR genes: update 1992.Semantic proximity Read ↗

X-linked isolated growth hormone deficiency: expanding the phenotypic spectrum of SOX3 polyalanine tract expansions.Semantic proximity Read ↗

Update on X-linked hypogammaglobulinemia with isolated growth hormone deficiency.Semantic proximity Read ↗

X-linked mental retardation.Semantic proximity Read ↗

The reduced expression of the HADH2 protein causes X-linked mental retardation, choreoathetosis, and abnormal behavior.Semantic proximity Read ↗

Type IA isolated growth hormone deficiency (IGHD) consistent with compound heterozygous deletions of 6.7 and 7.6 Kb at the GH1 gene locus.Semantic proximity Read ↗

Xq13.2q21.1 duplication encompassing the ATRX gene in a man with mental retardation, minor facial and genital anomalies, short stature and broad thorax.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.