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Del(3) (p25.3) without phenotypic effect.
  1. L A Knight,
  2. M H Yong,
  3. M Tan,
  4. I S Ng
  1. Department of Pathology, Singapore General Hospital.

    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.

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