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Article

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

Clinical dysmorphology - 1 Oct 2009

Burkitt Wright Emma M M, Perveen Rahat, Clayton Peter E, Hall Catherine M, Costa Teresa, Procter Annie M, Giblin Carol A, Donnai Dian, Black Graeme C

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Share to DNA Mutational Analysis
Share to Genes, X-Linked
Share to Human Growth Hormone

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Infant, Newborn

Share to Peptides

Share to SOXB1 Transcription Factors

Share to Trinucleotide Repeat Expansion

Source

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Identifiers

PMID: 19654509
DOI: 10.1097/MCD.0b013e32832d06f0
PMCID: PMC2763399

Genes

SOX3

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

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X-linked isolated growth hormone deficiency: expanding the phenotypic spectrum of SOX3 polyalanine tract expansions.PMID 19654509Read ↗

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