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Article

Atypical presentation of Denys-Drash syndrome in a female with a novel Wt1 gene mutation.

Birth defects original article series - 1 Jan 1996

Machin G A

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 9125334

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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

Atypical presentation of Denys-Drash syndrome in a female with a novel Wt1 gene mutation.PMID 9125334Read ↗

Clinical features and an atypical WT1 mutant site in a child with incomplete Denys-Drash syndrome.Semantic proximity Read ↗

A necropsy case of Denys-Drash syndrome with a WT1 mutation in exon 7.Semantic proximity Read ↗

Denys-Drash syndrome: Relating a clinical disorder to genetic alterations in the tumor suppressor gene WT1Semantic proximity Read ↗

WT1 mutations associated with incomplete Denys-Drash syndrome define a domain predicted to behave in a dominant-negative fashion.Semantic proximity Read ↗

WT1-related disorders: more than Denys-Drash syndrome.Semantic proximity Read ↗

Clinical presentation of DFNB1.Semantic proximity Read ↗

Clinical pictures and novel mutations of WT1-associated Denys-Drash syndrome in two Chinese children.Semantic proximity Read ↗

Highly variable clinical manifestations in a large family with a novel GATA2 mutation.Semantic proximity Read ↗

[Atypical presentation of MEN 1 syndrome].Semantic proximity Read ↗

Atypical clinical presentation of a WT1-related syndrome associated with a novel exon 6 gene mutation.Semantic proximity Read ↗

Clinical presentation of DFNA11 (MYO7A).Semantic proximity Read ↗

Atypical presentation of Dowling-Degos disease with novel and recurrent mutations in POFUT1.Semantic proximity Read ↗

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