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Article

[Identification of MYH9 gene mutation in a May-Hegglin anomaly family].

Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi - 1 Aug 2012

Gao Feng, Hao Ji-hong, Wang Zhen-lei

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Source

Identifiers

PMID: 23134864

Genes

MYH9

Provenance

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

Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Identification of MYH9 gene mutation in a May-Hegglin anomaly family].PMID 23134864Read ↗

Identification of a novel MYH9 mutation in a patient with May-Hegglin anomaly.Semantic proximity Read ↗

[Analysis of gene mutation in a family featuring autosomal dominant May-Hegglin anomaly].Semantic proximity Read ↗

[A non-familial May-Hegglin anomaly accompanying with MYH9 gene R1933X mutation and I1626V polymorphism].Semantic proximity Read ↗

A Trp33Arg mutation at exon 1 of the MYH9 gene in a Korean patient with May-Hegglin anomaly.Semantic proximity Read ↗

[Molecular diagnosis of a family with May-Hegglin anomaly].Semantic proximity Read ↗

Description of a novel mutation leading to MYH9-related disease.Semantic proximity Read ↗

[Clinical and molecular-biological study of a May-Hegglin anomaly family].Semantic proximity Read ↗

A case report of a family with MYH9 gene mutation-related disease in an ethnic minority group and literature review.Semantic proximity Read ↗

A case of MYH9 disorders caused by a novel mutation (p.K74E).Semantic proximity Read ↗

[Analysis of phenotype and pathogenic variant in a case of Heimler syndrome].Semantic proximity Read ↗

Adams-Oliver syndrome and familial MYH9 mutation.Semantic proximity Read ↗

Somatic mosaicism in MYH9 disorders: the need to carefully evaluate apparently healthy parents.Semantic proximity Read ↗

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