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DNA analysis of two patients with a non-fluorescent Y chromosome.

Abstract
Results of DNA study on two patients of gonadal dysgenesis with a 45,X/46,X,Ynf (non-fluorescent Y chromosome) karyotype are described. In one patient who developed gonadoblastoma, all 12 loci on the non-fluorescent part of Yq were detected. Another patient did not have gonadoblastoma at 20 years, and only the proximal 6 loci out of 12 were detected.
AuthorsT Sekine, K Fukutani, T Motegi, H Hayakawa, T Tamura, S Nagafuchi, Y Nakahori, Y Nakagome
JournalThe Japanese journal of human genetics (Jpn J Hum Genet) Vol. 37 Issue 2 Pg. 157-62 (Jun 1992) ISSN: 0916-8478 [Print] Japan
PMID1391971 (Publication Type: Case Reports, Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • DNA Probes
Topics
  • Adult
  • Child
  • Chromosome Banding
  • DNA Probes
  • Dysgerminoma (genetics)
  • Female
  • Fluorescence
  • Genital Neoplasms, Female (genetics)
  • Gonadal Dysgenesis (genetics)
  • Humans
  • Karyotyping
  • Y Chromosome

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