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46,XX disorder of sex development associated with skin abnormalities due to homozygous R-Spondin 1 loss of function mutation

Authors

  1. Correspondence to Dr Beatrice Anne; maglarne{at}gmail.com
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Citation

Divyasri N, Varma P, Kunnuru S, et al
46,XX disorder of sex development associated with skin abnormalities due to homozygous R-Spondin 1 loss of function mutation

Publication history

  • Accepted January 21, 2024
  • First published February 7, 2024.
Online issue publication 
February 07, 2024

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