Associated Papers
Clinical and genetic heterogeneity of congenital adrenal hypoplasia due to NR0B1 gene mutations.
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Gonadotropin-releasing hormone deficiency in the human (idiopathic hypogonadotropic hypogonadism and Kallmann's syndrome): pathophysiological and genetic considerations.
Seminara SB et al.
Endocrine Reviews, 1998
DAX1 mutations map to putative structural domains in a deduced three-dimensional model.
Zhang YH et al.
American Journal of Human Genetics, 1998
Electrostatic interactions in hirudin-thrombin binding.
Sharp KA
Biophysical Chemistry, 1996
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