DOI:
10.1055/s-00000072
Seminars in Reproductive Medicine
LinksClose Window
References
Fluck C, Deladoey J, Rutishauser K.
Phenotypic variability in familial combined pituitary hormone deficiency caused by a PROP1 gene mutation resulting in the substitution of Arg → Cys at codon 120 (R120C)
J Clin Endocrinol Metab 1998; 83: 3727-3734
We do not assume any responsibility for the contents of the web pages of other providers.