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Nobel deletion alleles carrying CYP21A1P/A2 chimeric genes in Brazilian patients with 21-hydroxylase deficiency
(Biomed Central LtdLondonInglaterra, 2010)
Genetic study of patients with dexamethasone-suppressible aldosteronism without the chimeric CYP11B1/CYP11B2 gene
(ENDOCRINE SOC, 2001)
Glucocorticoid-remediable aldosteronism is an inherited disorder caused by a chimeric gene duplication between the CYP11B1 (11 beta -hydroxylase) and CYP11B2 (aldosterone synthase) genes. The disorder is characterized by ...
A De Novo Mutation In Cyp21a2 Gene In A Case Of In Vitro Fertilization
(Elsevier Inc., 2015)
H28+C insertion in the CYP21 gene: A novel frameshift mutation in a Brazilian patient with the classical form of 21-hydroxylase deficiency
(Endocrine SocChevy ChaseEUA, 2001)