RT Journal Article
SR Electronic
T1 Del(3) (p25.3) without phenotypic effect.
JF Journal of Medical Genetics
JO J Med Genet
FD BMJ Publishing Group Ltd
SP 994
OP 995
DO 10.1136/jmg.32.12.994
VO 32
IS 12
A1 L A Knight
A1 M H Yong
A1 M Tan
A1 I S Ng
YR 1995
UL http://jmg.bmj.com/content/32/12/994.abstract
AB 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.