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1.
Lack of correlation between phenotype and genotype in untreated 21-hydroxylase-deficient Indonesian patients.
Clin Endocrinol (Oxf)
; 71(5): 628-35, 2009 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-19226270
2.
Insight into mutation-induced activation of the luteinizing hormone receptor: molecular simulations predict the functional behavior of engineered mutants at M398.
Mol Endocrinol
; 18(6): 1499-508, 2004 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-15016840
3.
Differential inhibition of 17alpha-hydroxylase and 17,20-lyase activities by three novel missense CYP17 mutations identified in patients with P450c17 deficiency.
J Clin Endocrinol Metab
; 87(12): 5714-21, 2002 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-12466376
4.
Isolated 17,20-lyase deficiency due to the cytochrome b5 mutation W27X.
J Clin Endocrinol Metab
; 95(3): 994-9, 2010 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-20080843
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