The prevalence of digenic mutations in patients with normosmic hypogonadotropic hypogonadism and Kallmann syndrome

Fertility and Sterility

Volumn 96, Issue 6, 2011, Pages

  Quaynor, Samuel D ^a   Kim, Hyung Goo ^a   Cappello, Elizabeth M ^a   Williams, Tiera ^a   Chorich, Lynn P ^a   Bick, David P ^b   Sherins, Richard J ^c   Layman, Lawrence C ^a  

^a MEDICAL COLLEGE OF GEORGIA   (United States)

^b MEDICAL COLLEGE OF WISCONSIN   (United States)

^c Columbia Fertility Associates   (United States)

Author keywords

Digenic mutations; idiopathic hypogonadotropic hypogonadism; Kallmann syndrome

Indexed keywords

KAINIC ACID;

ARTICLE; CLINICAL ARTICLE; CONTROLLED STUDY; DNA DETERMINATION; DNA SEQUENCE; FEMALE; GENE MUTATION; HETEROZYGOTE; HUMAN; HYPOGONADOTROPIC HYPOGONADISM; KALLMANN SYNDROME; MALE; PHENOTYPE; PREVALENCE; PRIORITY JOURNAL; SEQUENCE ANALYSIS;

EID: 82455162354     PISSN: 00150282     EISSN: 15565653     Source Type: Journal    
DOI: 10.1016/j.fertnstert.2011.09.046     Document Type: Article

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