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Whole exome sequencing reveals copy number variants in individuals with disorders of sex development

Rajini Sreenivasan1, Katrina Bell2, Jocelyn van den Bergen2

  • 1Murdoch Children's Research Institute, Melbourne, Australia; Department of Paediatrics, University of Melbourne, Melbourne, Australia.

Molecular and Cellular Endocrinology
|January 20, 2022
PubMed

Keywords:
Androgen receptorComplete androgen insensitivity syndromeCopy number variationDisorders of sex developmentExome sequencing

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