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Absence of Y specific DNA sequences in two siblings with 46XX hermaphroditism.

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  • معلومة اضافية
    • بيانات النشر:
      British Medical Journal Publishing Group
    • الموضوع:
      1989
    • Collection:
      HighWire Press (Stanford University)
    • نبذة مختصرة :
      We report two siblings with 46XX hermaphroditism in whom we were unable to show the presence of Y specific DNA sequences using the DNA probes Y-190, GMGY-7, pHY2.1, pDP34, and 27a. We conclude that an autosomal or X chromosome gene mutation is the most likely mechanism of inheritance in this family with 46XX hermaphroditism.
    • File Description:
      text/html
    • Relation:
      http://adc.bmj.com/cgi/content/short/64/8/1185; http://dx.doi.org/10.1136/adc.64.8.1185
    • الرقم المعرف:
      10.1136/adc.64.8.1185
    • الدخول الالكتروني :
      http://adc.bmj.com/cgi/content/short/64/8/1185
      https://doi.org/10.1136/adc.64.8.1185
    • Rights:
      Copyright (C) 1989, BMJ Publishing Group Ltd
    • الرقم المعرف:
      edsbas.2799CD8E