Results 71 to 80 of about 338 (94)

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

Fertility and Sterility, 2011
Hyung-Goo Kim
exaly  

Identification of HESX1 mutations in Kallmann syndrome

Fertility and Sterility, 2013
Hyung-Goo Kim
exaly  

Kallmann syndrome in women: from genes to diagnosis and treatment

Gynecological Endocrinology, 2013
Blazej Meczekalski
exaly  

Kallmann syndrome associated with choanal atresia

Clinical Genetics, 1987
Jan M Friedman
exaly  

Evidence that FGFR1 loss-of-function mutations may cause variable skeletal malformations in patients with Kallmann syndrome

Advances in Medical Sciences, 2012
Katarzyna Jarzabek, Slawomir Wolczynski
exaly  

Kallmann's syndrome and chemosensory evoked potentials

European Archives of Oto-Rhino-Laryngology, 1991
Thomas Hummel
exaly