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Article

SHOX gene in Leri-Weill syndrome and in idiopathic short stature.

Journal of endocrinological investigation - 1 Oct 2001

Bernasconi S, Mariani S, Falcinelli C, Milioli S, Iughetti L, Forabosco A

Abstract excerpt

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Topics

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 11716161
DOI: 10.1007/BF03343919

Genes

SHOX

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

SHOX gene in Leri-Weill syndrome and in idiopathic short stature.PMID 11716161Read ↗

SHOX defects in idiopathic short stature.Semantic proximity Read ↗

Short stature due to SHOX deficiency: genotype, phenotype, and therapy.Semantic proximity Read ↗

SHOX in short stature syndromes.Semantic proximity Read ↗

Short stature and dysmorphology associated with defects in the SHOX gene.Semantic proximity Read ↗

SHOX gene defects and selected dysmorphic signs in patients of idiopathic short stature and Léri-Weill dyschondrosteosis.Semantic proximity Read ↗

The short stature homeobox gene SHOX is involved in skeletal abnormalities in Turner syndrome.Semantic proximity Read ↗

Genotype-Phenotype Relationship in Patients and Relatives with SHOX Region Anomalies in the French Population.Semantic proximity Read ↗

Clinical and radiological characteristics of 22 children with SHOX anomalies and familial short stature suggestive of Léri-Weill Dyschondrosteosis.Semantic proximity Read ↗

Detection of SHOX Gene Variations in Patients with Skeletal Abnormalities with or without Short StatureSemantic proximity Read ↗

[From gene to disease; from SHOX to Lèri-Weill dyschondrosteosis, Turner syndrome and idiopathic short stature].Semantic proximity Read ↗

Genotypes and phenotypes of children with SHOX deficiency in France.Semantic proximity Read ↗

SHOX at a glance: from gene to protein.Semantic proximity Read ↗

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