Del(3) (p25.3) without phenotypic effect.
Open Access
- 1 December 1995
- journal article
- case report
- Published by BMJ in Journal of Medical Genetics
- Vol. 32 (12) , 994-995
- https://doi.org/10.1136/jmg.32.12.994
Abstract
A terminal deletion of chromosome 3 at p25.3 was observed during prenatal diagnosis. A similar deletion is also present in the phenotypically normal mother. The deletion was confirmed by FISH. The breakpoint is distal to the region responsible for the 3p- syndrome. A normal baby girl was born with no apparent phenotypic abnormalities.Keywords
This publication has 3 references indexed in Scilit:
- Molecular genetic analysis of the 3p — syndromeHuman Molecular Genetics, 1994
- Infant with del(3) (p25-pter): Karyotype-phenotype correlation and review of previously reported casesAmerican Journal of Medical Genetics, 1992
- Terminal deletion of the short arm of chromosome 3Journal of Human Genetics, 1992