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Article

A multi-exon deletion within WWOX is associated with a 46,XY disorder of sex development

9 Nov 2011

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Share to Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 22071891
DOI: 10.1038/ejhg.2011.204

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Related research

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A multi-exon deletion within WWOX is associated with a 46,XY disorder of sex developmentPMID 22071891Read ↗

The Role of WWOX Gene Variant in Hypospadias and 46,XY Disorders of Sexual Development.Semantic proximity Read ↗

The WWOX gene in brain development and pathologySemantic proximity Read ↗

The fragile site WWOX gene and the developing brain.Semantic proximity Read ↗

W44X mutation in the WWOX gene causes intractable seizures and developmental delay: a case report.Semantic proximity Read ↗

Loss of Wwox Perturbs Neuronal Migration and Impairs Early Cortical DevelopmentSemantic proximity Read ↗

The supposed tumor suppressor gene WWOX is mutated in an early lethal microcephaly syndrome with epilepsy, growth retardation and retinal degeneration.Semantic proximity Read ↗

A heterozygous germline deletion within USP8 causes severe neurodevelopmental delay with multiorgan abnormalitiesSemantic proximity Read ↗

Genetic and epigenetic insights into Werner SyndromeSemantic proximity Read ↗

Molecular Biology of the WWOX Gene That Spans Chromosomal Fragile Site FRA16D.Semantic proximity Read ↗

Novel homozygous mutation in the WWOX gene causes seizures and global developmental delay: Report and reviewSemantic proximity Read ↗

WWOX at the crossroads of cancer, metabolic syndrome related traits and CNS pathologies.Semantic proximity Read ↗

A 600 kb triplication in the cat eye syndrome critical region causes anorectal, renal and preauricular anomalies in a three-generation familySemantic proximity Read ↗

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