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Article

SHOX defects in idiopathic short stature.

Journal of pediatric endocrinology & metabolism : JPEM - 1 Dec 2002

Ogata Tsutomu

Abstract excerpt

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Topics

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Share to Body Height
Share to Gene Deletion
Share to SHOX gene
Share to Growth Disorders

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Homeodomain Proteins

Share to Mutation

Share to Short Stature Homeobox Protein

Source

Identifiers

PMID: 12511003

Genes

SHOX

Provenance

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

Related research

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SHOX defects in idiopathic short stature.PMID 12511003Read ↗

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

SHOX gene in Leri-Weill syndrome and in idiopathic short stature.Semantic proximity Read ↗

Prevalence of SHOX haploinsufficiency among short statured childrenSemantic proximity Read ↗

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

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

SHOX in short stature syndromes.Semantic proximity Read ↗

Novel heterozygous mutation in the SHOX gene leading to familial idiopathic short stature: A case report and literature review.Semantic proximity Read ↗

SHOX deficiency in short Taiwanese children: A single-center experience.Semantic proximity Read ↗

High incidence of SHOX anomalies in individuals with short stature.Semantic proximity Read ↗

The novel human SHOX allelic variant database.Semantic proximity Read ↗

ACMG practice guideline: genetic evaluation of short stature.Semantic proximity Read ↗

New developments in the genetic diagnosis of short stature.Semantic proximity Read ↗

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