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Article

Molecular, cytogenetic, and clinical characterisation of six XX males including one prenatal diagnosis.

1 Sept 1998

Abstract excerpt

Cytogenetic analysis, fluorescent in situ hybridisation (FISH), and molecular amplification have been used to characterise the transfer of Yp fragments to Xp22.3 in six XX males. PCR amplification of the genes SRY, RPS4Y, ZFY, AMELY, KALY, and DAZ and of several other markers along the Y chromosome short and long arms indicated the presence of two different breakpoints in the Y fragment. However, the clinical...

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Identifiers

PMID: 9733030
DOI: 10.1136/jmg.35.9.727

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