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Article

Adams-Oliver syndrome and familial MYH9 mutation.

Pediatrics international : official journal of the Japan Pediatric Society - 1 Jun 2012

Uyeda Tomomi, Echizenya Taketora, Eto Shuji, Ohtani Katsuki, Sato Takumi, Takahashi Tohru, Ito Etsuro, Yonesaka Susumu, Kunishima Shinji

Abstract excerpt

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Topics

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Share to Limb Deformities, Congenital
Share to Ectodermal Dysplasia
Share to MYH9 gene
Share to Infant, Newborn

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 22631568
DOI: 10.1111/j.1442-200X.2011.03466.x

Genes

MYH9

Provenance

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

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Adams-Oliver syndrome and familial MYH9 mutation.PMID 22631568Read ↗

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

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

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

Adams-Oliver syndrome, a family with dominant inheritance and a severe phenotype.Semantic proximity Read ↗

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

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

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

Familial adenomatous polyposis and MYH.Semantic proximity Read ↗

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

Adams-Oliver syndrome: clinical description of a four-generation family and exclusion of five candidate genes.Semantic proximity Read ↗

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

DKC1 mutation causing different phenotypes in a family with X-linked Hoyeraal-Hreidarsson syndromeSemantic proximity Read ↗

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