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Related Experiment Videos

Ring chromosome 15 syndrome.

J P Fryns, J Timmermans, F D Hondt

    Human Genetics
    |September 2, 1979
    PubMed
    Summary
    This summary is machine-generated.

    Ring chromosome 15 is a rare genetic condition. Patients typically exhibit intellectual disability, growth deficiencies, and distinct facial and limb features.

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    Area of Science:

    • Genetics
    • Clinical Genetics
    • Human Genetics

    Background:

    • Ring chromosome 15 is a rare chromosomal abnormality.
    • Previous literature describes limited cases, necessitating further characterization.