4 Article(s)Download |
PMID | Title | Pub. Year | #Total Relationships |
1 | 19347184 | High frequency of Q318X mutation in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency in northeast Brazil. | 2009 Feb | 1 |
2 | 14502362 | Phenotype and genotype correlation of the microconversion from the CYP21A1P to the CYP21A2 gene in congenital adrenal hyperplasia. | 2003 Oct | 1 |
3 | 10602386 | Restoration of adrenal steroidogenesis by adenovirus-mediated transfer of human cytochromeP450 21-hydroxylase into the adrenal gland of21-hydroxylase-deficient mice. | 1999 Nov | 1 |
4 | 9132494 | Characterisation of CAH alleles with non-radioactive DNA single strand conformation polymorphism analysis of the CYP21 gene. | 1997 Mar | 1 |