Your search returned 2 results.

Results
	1.	Classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency: a cross-sectional study of factors involved in bone mineral density. [electronic resource] by de Almeida Freire, Patrícia Oliveira de Lemos-Marini, Sofia Helena Valente Maciel-Guerra, Andréa Trevas Morcillo, André Moreno Matias Baptista, Maria Tereza de Mello, Maricilda Palandi Guerra, Gil Producer: 20040702 In: Journal of bone and mineral metabolism vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Loss-of-function mutations in the genes encoding prokineticin-2 or prokineticin receptor-2 cause autosomal recessive Kallmann syndrome. [electronic resource] by Abreu, Ana Paula Trarbach, Ericka Barbosa de Castro, Margaret Frade Costa, Elaine Maria Versiani, Beatriz Matias Baptista, Maria Tereza Garmes, Heraldo Mendes Mendonca, Berenice Bilharinho Latronico, Ana Claudia Producer: 20081124 In: The Journal of clinical endocrinology and metabolism vol. 93 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

Refine your search