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Article

Kallmann syndrome due to a translocation resulting in an X/Y fusion gene

1 Aug 1992

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Identifiers

PMID: 1302031
DOI: 10.1038/ng0892-337

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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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Kallmann syndrome due to a translocation resulting in an X/Y fusion genePMID 1302031Read ↗

Structure of the X–linked Kallmann syndrome gene and its homologous pseudogene on the Y chromosomeSemantic proximity Read ↗

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Familial X;Y translocation with distinct phenotypic consequences: Characterization using FISH and array CGH.Semantic proximity Read ↗

The Gene for Bazex-Dupré-Christol Syndrome Maps to Chromosome XqSemantic proximity Read ↗

Retinal mosaicism in a girl with an X-Y translocation.Semantic proximity Read ↗

Familial X/Y Translocation Encompassing ARSE in Two Moroccan Siblings with Sensorineural Deafness.Semantic proximity Read ↗

Translocation 19;Y in a child with Bannayan-Zonana phenotype.Semantic proximity Read ↗

Kallmann’s syndrome, a neuronal migration defectSemantic proximity Read ↗

SHOX duplications found in some cases with type I Mayer-Rokitansky-Kuster-Hauser syndromeSemantic proximity Read ↗

A prenatally ascertained X;Y translocation characterized using conventional and molecular cytogenetics.Semantic proximity Read ↗

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