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Molecular analysis of CYP21 and C4 genes in Brazilian families with the classical form of steroid 21-hydroxylase deficiency

deAraujo, M; Sanches, MR; Suzuki, LA; Guerra, G; Farah, SB; deMello, MP (Assoc Bras Divulg CientificaSao PauloBrasil, 1996)

Mutation distribution and CYP21/C4 locus variability in Brazilian families with the classical form of the 21-hydroxylase deficiency

Paulino, LC; Araujo, M; Guerra, G; Marini, SHVL; De Mello, MP (Scandinavian University PressOsloNoruega, 1999)

[11beta-hydroxylase Deficiency].

Mello, Maricilda Palandi; Penachioni, Junia Yara; Amaral, Fernando C do; Castro, Margaret de (2004)

Molecular Analysis Of Cyp21 And C4 Genes In Brazilian Families With The Classical Form Of Steroid 21-hydroxylase Deficiency.

de-Araujo, M; Sanches, M R; Suzuki, L A; Guerra, G; Farah, S B; de-Mello, M P (1996)

17-hydroxyprogesterone deficiency as a cause of sexual infantilism and arterial hypertension: Laboratory and molecular diagnosis - a case report

Benetti-Pinto, CL; Vale, D; Garmes, H; Bedone, A (Parthenon Publishing GroupLancasterInglaterra, 2007)

21-hydroxylase deficiency transiently mimicking combined 21- and 11 beta-hydroxylase deficiency

Tonetto-Fernandes, V; Lemos-Marini, SHV; De Mello, MP; Ribeiro, LM; Kater, CE (Walter De Gruyter GmbhBerlinAlemanha, 2008)

Female Pseudohermaphroditism Due To Classical 21-hydroxylase Deficiency In A Girl With Turner Syndrome.

Maciel-Guerra, A T; Guerra, G; Marini, S H; Matias Baptista, M T; Marques-de-Faria, A P (1997)

Classical Congenital Adrenal Hyperplasia Due To 21-hydroxylase Deficiency: A Cross-sectional Study Of Factors Involved In Bone Mineral Density.

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 (2003)

H28+C insertion in the CYP21 gene: A novel frameshift mutation in a Brazilian patient with the classical form of 21-hydroxylase deficiency

Lau, IF; Soardi, FC; Lemos-Marini, SHV; Guerra, G; Baptista, MTM; De Mello, MP (Endocrine SocChevy ChaseEUA, 2001)

H28+c Insertion In The Cyp21 Gene: A Novel Frameshift Mutation In A Brazilian Patient With The Classical Form Of 21-hydroxylase Deficiency.

Lau, I F; Soardi, F C; Lemos-Marini, S H; Guerra Jr, G; Baptista, M T; De Mello, M P (2001)

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