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pro vyhledávání: '"Kelsey R. Porter"'
Autor:
Samuel D. Quaynor, Lynn P. Chorich, Maggie E. Bosley, Lawrence C. Layman, Kelsey R. Porter, Megan E. Sullivan, Richard S. Cameron, Jeong Hyeon Choi, Hyung Goo Kim, Soo-Hyun Kim, Christina G. Duckworth
The genetic basis is unknown for ∼60% of normosmic hypogonadotropic hypogonadism (nHH)/Kallmann syndrome (KS). DNAs from (17 male and 31 female) nHH/KS patients were analyzed by targeted next generation sequencing (NGS) of 261 genes involved in hyp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2a4ee07011ecaea8f6ab8f646bd4b6a6
