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Related Experiment Videos

The 11q-- syndrome: another case report

M T Mulcahy, J Jenkyn

    Human Genetics
    |April 15, 1977
    PubMed
    Summary
    This summary is machine-generated.

    This study details a female infant with a 46,XX,del(11)(q23) karyotype. Findings support a potential new syndrome, del(11q), based on clinical and developmental comparisons.

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    Annales de genetique·1992
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    Chromosome abnormalities detected in chorionic villus biopsies of failing pregnancies in a subfertile population.

    British journal of obstetrics and gynaecology·1991
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    Tyrosinase positive albinism with familial 46,XY,t(2;4) (q31.2;q31.22) balanced translocation.

    Journal of medical genetics·1991
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    The American journal of pediatric hematology/oncology·1991
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    Another case of completely discordant findings at CVS.

    Prenatal diagnosis·1989
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    Deletion of chromosome 5q and familial adenomatous polyposis.

    Journal of medical genetics·1989

    Area of Science:

    • Genetics
    • Pediatrics
    • Clinical Medicine

    Background:

    • Chromosome 11q23 deletions are rare genetic abnormalities.
    • These deletions can lead to a range of developmental and clinical issues.