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Related Experiment Videos

Del(3) (p25.3) without phenotypic effect

L A Knight1, M H Yong, M Tan

  • 1Department of Pathology, Singapore General Hospital.

Journal of Medical Genetics
|December 1, 1995
PubMed
Summary
This summary is machine-generated.

A terminal deletion on chromosome 3 at p25.3 was detected during prenatal diagnosis in a phenotypically normal mother and her baby. The deletion did not cause abnormalities, indicating a potentially benign finding in this case.

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Area of Science:

  • Genetics
  • Prenatal Diagnosis
  • Cytogenetics

Background:

  • Terminal deletions of chromosome 3 can lead to various genetic syndromes.
  • The 3p- syndrome is associated with a specific deletion region on chromosome 3.
  • Prenatal diagnosis allows for the identification of chromosomal abnormalities before birth.