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Article

Precise localisation of 3p25 breakpoints in four patients with the 3p-syndrome.

1 Oct 1996

Abstract excerpt

In patients with the 3p-syndrome, hemizygous deletion of 3p25-pter is associated with profound growth failure, characteristic facial features, and mental retardation. We performed a molecular genetic analysis of 3p25 breakpoints in four patients with the 3p- syndrome, and a fifth patient with a more complex abnormality, 46,XY,der(3)t(3;?)(p25.3;?). EBV transformed lymphoblasts from each of the patients were...

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Identifiers

PMID: 8933338
DOI: 10.1136/jmg.33.10.842

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Source receipt: pubmed, retrieved 7 Sept 2026.

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