TY - JOUR T1 - Del(3) (p25.3) without phenotypic effect. JF - Journal of Medical Genetics JO - J Med Genet SP - 994 LP - 995 DO - 10.1136/jmg.32.12.994 VL - 32 IS - 12 AU - L A Knight AU - M H Yong AU - M Tan AU - I S Ng Y1 - 1995/12/01 UR - http://jmg.bmj.com/content/32/12/994.abstract N2 - 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. ER -