Results 111 to 120 of about 2,707 (125)
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Evidence That FGFR1 Loss-of-Function Mutations May Cause Variable Skeletal Malformations in Patients With Kallmann Syndrome

Advances in Medical Sciences, 2012
Katarzyna Jarzabek   +2 more
exaly  

Craniofacial Morphology in Patients With Kallmann's Syndrome With and Without Cleft Lip and Palate

Cleft Palate-Craniofacial Journal, 1997
Inger Kjaer   +2 more
exaly  

A Fertile Male Patient With Kallmann Syndrome and Two Missense Mutations in the KAL1 Gene

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

Renal Dysgenesis and KAL1 Gene Defects in Patients With Sporadic Kallmann Syndrome

Fertility and Sterility, 2007
Bessie E Spiliotis   +2 more
exaly  

Kallmann's Syndrome and Chemosensory Evoked Potentials

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

Gonadotropin Ovulation Induction and Pregnancies in Women With Kallmann's Syndrome

Gynecological Endocrinology, 1998
C Papadias   +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
Brunella Franco   +2 more
exaly  

Histopathology of Olfactory Mucosa in Kallmann's Syndrome

Annals of Otology, Rhinology and Laryngology, 1993
James E Schwob   +2 more
exaly  

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