PT - JOURNAL ARTICLE AU - L A Knight AU - M H Yong AU - M Tan AU - I S Ng TI - Del(3) (p25.3) without phenotypic effect. AID - 10.1136/jmg.32.12.994 DP - 1995 Dec 01 TA - Journal of Medical Genetics PG - 994--995 VI - 32 IP - 12 4099 - http://jmg.bmj.com/content/32/12/994.short 4100 - http://jmg.bmj.com/content/32/12/994.full SO - J Med Genet1995 Dec 01; 32 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.