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Keyword:
Congenital adrenal hyperplasia
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2+0 CYP21A2 deletion carrier — a limitation of the genetic testing and counseling: A case report
8/5/2021 2:37:05 PM |
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Turner syndrome with SRY gene and non-classical congenital adrenal hyperplasia: A case report
3/30/2021 8:56:50 AM |
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