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Case Reports

Persistent Müllerian Duct Syndrome Associated with Irreducible Inguinal Hernia, Bilateral Cryptorchidism and Testicular Neoplasia: a Case Report

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Pages 119-120 | Published online: 11 Mar 2016

References

  • Imbeaud S., Belvbille C., Messika-Zeitoun L. et al. A 27 basepair deletion of THA antimullerian type II receptor gene is the most common cause of THA persistent mullerian duct syndrome. Hum Mol Genet, 1996, 5: 1269–77.
  • Teixeira J., Maheswaran S., Donahoe P. K. Mullerian Inhibiting Substance A: a case report. Instructive Developmental Hormone with Diagnostic and Possible Therapeutic Applications. Endocr Rev, 2001, 22: 657–74.
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