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Article

A family of pseudohypoparathyroidism type Ia with an 850-kb submicroscopic deletion encompassing the whole GNAS locus.

American journal of medical genetics. Part A - 1 Jan 2012

Mitsui Toshikatsu, Nagasaki Keisuke, Takagi Masaki, Narumi Satoshi, Ishii Tomohiro, Hasegawa Tomonobu

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Share to Chromogranins
Share to Comparative Genomic Hybridization
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to GTP-Binding Protein alpha Subunits, Gs

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Source

Identifiers

PMID: 22140064
DOI: 10.1002/ajmg.a.34393

Genes

GNAS

Provenance

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

Related research

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A family of pseudohypoparathyroidism type Ia with an 850-kb submicroscopic deletion encompassing the whole GNAS locus.PMID 22140064Read ↗

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A Novel GNAS Mutation in a Patient with Ia Pseudohypoparathyroidism (iPPSD2) Phenotype.Semantic proximity Read ↗

GNAS Spectrum of Disorders.Semantic proximity Read ↗

Identification of a novel mutation in pseudohypoparathyroidism type Ia in a Chinese family: A case report.Semantic proximity Read ↗

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An update on the clinical and molecular characteristics of pseudohypoparathyroidism.Semantic proximity Read ↗

Familial investigation of two cases of pseudohypoparathyroidism.Semantic proximity Read ↗

A novel mutation in a case of pseudohypoparathyroidism type Ia.Semantic proximity Read ↗

A de novo 50-bp GNAS Intragenic Duplication in a Patient with Pseudohypoparathyroidism Type 1a.Semantic proximity Read ↗

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