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Inherited mutation of the luteinizing hormone/choriogonadotropin receptor (LHCGR) in empty follicle syndrome

By Kemal O. Yariz, Tom Walsh, Asli Uzak, Michail Spiliopoulos, Duygu Duman, Gogsen Onalan, Mary-Claire King and Mustafa Tekin
Publisher: Elsevier BV
Year: 2011
DOI identifier: 10.1016/j.fertnstert.2011.05.057
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Provided by: MUCC (Crossref)
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