Results 71 to 80 of about 101 (87)

Kallmann syndrome in women: from genes to diagnosis and treatment

Gynecological Endocrinology, 2013
Blażej Meczekalski, Krzysztof Katulski   +1 more
exaly  

Kallmann syndrome associated with choanal atresia

Clinical Genetics, 1987
VÍCTOR R Klein, Jan M Friedman, Orval E Brown   +2 more
exaly  

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

Advances in Medical Sciences, 2012
K Jarzabek, Slawomir Wolczynski, M L Kottler   +2 more
exaly  

Craniofacial Morphology in Patients with Kallmann's Syndrome with and without Cleft Lip and Palate

Cleft Palate-Craniofacial Journal, 1997
Kirsten Mølsted, Inger Kjær
exaly  

Kallmann's syndrome and chemosensory evoked potentials

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

Renal dysgenesis and KAL1 gene defects in patients with sporadic Kallmann syndrome

Fertility and Sterility, 2007
Vasiliki Koika, Assimina Galli-Tsinopoulou, Bessie E Spiliotis   +2 more
exaly  

A fertile male patient with Kallmann syndrome and two missense mutations in the KAL1 gene

Fertility and Sterility, 2011
Zhuo Liu, Shaogang Wang, Jihong Liu
exaly  

WDR11‐mediated Hedgehog signalling defects underlie a new ciliopathy related to Kallmann syndrome

EMBO Reports, 2018
Masatake Araki, Kimi Araki, Hyun-Taek Kim   +2 more
exaly  

Variable penetrance of hypogonadism in a sibship with Kallmann syndrome due to a deletion of the KAL gene

American Journal of Medical Genetics Part A, 1995
Giancarlo Parenti, S Di Maio, Maria Pia Sperandeo   +2 more
exaly  

Heterogeneity of Kallmann's syndrome

Clinical Genetics, 1985
M Hermanussen, W G Sippell
exaly