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Article

Intronic mutation in the growth hormone receptor gene in a Peruvian girl with Laron syndrome.

Journal of pediatric endocrinology & metabolism : JPEM - 1 Jan 2000

Shevah O, Nunez O, Rubinstein M, Laron Z

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 12199333
DOI: 10.1515/jpem.2002.15.7.1039

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.

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Intronic mutation in the growth hormone receptor gene in a Peruvian girl with Laron syndrome.PMID 12199333Read ↗

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A Recurrent Mutation in Growth Hormone Receptor (GHR) Gene Underlying Laron-type Dwarfism in a Pakistani Family.Semantic proximity Read ↗

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