Clinical and molecular characterization of a large sample of patients with hypogonadotropic hypogonadism

Fertility and Sterility

Volumn 85, Issue 3, 2006, Pages 706-713

  Bhagavath, Balasubramanian ^a   Podolsky, Robert H ^a   Ozata, Metin ^b   Bolu, Erol ^c   Bick, David P ^d   Kulharya, Anita ^a   Sherins, Richard J ^e   Layman, Lawrence C ^a  

^a MEDICAL COLLEGE OF GEORGIA   (United States)

^b GATA HAYDARPASA TRAINING HOSPITAL   (Turkey)

^c GULHANE SCHOOL OF MEDICINE   (Turkey)

^d UNIVERSITY OF WISCONSIN MADISON   (United States)

^e GENETICS AND IVF INSTITUTE   (United States)

Author keywords

Gene mutation; Gonadotropin releasing hormone deficiency; Idiopathic hypogonadotropic hypogonadism; Kallmann syndrome

Indexed keywords

GONADORELIN RECEPTOR; KALLMANN SYNDROME 1 PROTEIN; PROTEIN; UNCLASSIFIED DRUG;

ADULT; ANOSMIA; AUTOSOMAL RECESSIVE INHERITANCE; CONTROLLED STUDY; CORRELATION ANALYSIS; CRYPTORCHISM; DISEASE ASSOCIATION; DISEASE SEVERITY; FEMALE; GENE EXPRESSION; GENE MUTATION; GENOTYPE; HUMAN; HYPOGONADOTROPIC HYPOGONADISM; KARYOTYPE; MAJOR CLINICAL STUDY; MALE; PRIORITY JOURNAL; REVIEW; SMELLING;

EID: 32944478440     PISSN: 00150282     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.fertnstert.2005.08.044     Document Type: Article

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