Aufsatz(elektronisch)#1Januar 1998
The low frequency of Kallmann syndrome (KAL) gene mutations in humans with hypogonadotropic hypogonadism suggests non-x linked modes of inheritance
In: Journal of the Society for Gynecologic Investigation: official publication of the Society for Gynecologic Investigation, Band 5, Heft 1, S. 93A-93A
ISSN: 1556-7117