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Leydig cell hypoplasia due to inactivating luteinizing hormone/chorionic gonadotropin receptor gene mutation presenting as a 46,XY DSD.

Advances in experimental medicine and biology - 1 Jan 2011

Sinha Sunil K, Bhangoo Amrit, Ten Svetlana, Gromoll Joerg

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PMID: 21691974
DOI: 10.1007/978-1-4419-8002-1_32

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