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Article

Xp22.3 deletions in isolated familial Kallmann's syndrome.

1 Apr 1993

Abstract excerpt

Several familial cases of Kallmann's syndrome (KS) have been reported, among which the X-chromosome-linked mode of inheritance is the most frequent. The gene responsible for the X-linked KS has been localized to the terminal part of the X-chromosome short arm (Xp22.3 region), immediately proximal to the steroid sulfatase gene responsible for X-linked ichthyosis. Large deletions of this region have been previously...

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Identifiers

PMID: 8473391
DOI: 10.1210/jcem.76.4.8473391

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Xp22.3 deletions in isolated familial Kallmann's syndrome.PMID 8473391Read ↗

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A clinical and genetic study of X-linked recessive ichthyosis and contiguous gene defectsSemantic proximity Read ↗

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