Unbalanced 13q/21q translocation: A revised study of the case previously reported as 21-monosomy View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

1976-01

AUTHORS

Tatsuro Ikeuchi, Ikuko Kondo, Motomichi Sasaki, Yasuhiko Kaneko, Susumu Kodama, Tsukasa Hattori

ABSTRACT

Reexamination was made on a male infant previously reported as 21-monosomy. Extensive chromosome banding analyses in the patient and parents disclosed an unbalanced de novo translocation between chromosomes 13 and 21. The patient's karyotype was interpreted as 45,XY,--13,--21+der(13),t(13;21) (q2 or 3;q1 or 2)pat. The patient showed many clinical features characteristic of 13q--syndrome. More... »

PAGES

327-330

References to SciGraph publications

  • 1976-01. Does full monosomy 21 exist? in HUMAN GENETICS
  • 1975-03. A male infant with monosomy 21 in HUMANGENETIK
  • Identifiers

    URI

    http://scigraph.springernature.com/pub.10.1007/bf00286861

    DOI

    http://dx.doi.org/10.1007/bf00286861

    DIMENSIONS

    https://app.dimensions.ai/details/publication/pub.1041115464

    PUBMED

    https://www.ncbi.nlm.nih.gov/pubmed/964993


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