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Article

Identification of a novel MYH9 mutation in a patient with May-Hegglin anomaly.

Pediatric blood & cancer - 1 Dec 2006

Otsubo Keisuke, Kanegane Hirokazu, Nomura Keiko, Ogawa Jiro, Miyawaki Toshio, Kunishima Shinji

Abstract excerpt

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 16642488
DOI: 10.1002/pbc.20879

Genes

MYH9

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.

Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

Identification of a novel MYH9 mutation in a patient with May-Hegglin anomaly.PMID 16642488Read ↗

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

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

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

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

Identification of a novel MYH9-related disease-associated mutation with multiple faintly staining Döhle-like bodies.Semantic proximity Read ↗

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

Novel variant of MYH9 associated with mild evaluation of MYH9 related disorder in a Chinese family.Semantic proximity Read ↗

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

A sporadic MYH9-related disease in a Chinese boy with p.A95T mutation.Semantic proximity Read ↗

A novel MYH9 variant in a Chinese patient with MYH9 related diseaseSemantic proximity Read ↗

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

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