Female pseudohermaphroditism caused by a novel homozygous missense mutation of the GR gene (2002)
- Authors:
- Mendonça, Berenice Bilharinho de
- Leite, Maristela V. - Universidade Federal do Rio Grande do Norte (UFRN)
- Castro, Margaret de
- Kino, Tomoshige - National Institutes of Health (NIH)
- Elias, Lucila L. K.
- Bachega, Tania A. S.
- Arnhold, Ivo J. P.
- Chrousos, George P. - National Institutes of Health (NIH)
- Latronico, Ana Claudia
- USP affiliated authors: MENDONCA, BERENICE BILHARINHO DE - FM ; CASTRO, MARGARET DE - FMRP
- Unidades: FM; FMRP
- Subjects: ENDOCRINOLOGIA; MUTAÇÃO GENÉTICA
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: The Journal of Clinical Endocrinology & Metabolism
- ISSN: 0021-972X
- Volume/Número/Paginação/Ano: v. 87, n. 4, p. 1805-1809, 2002
-
ABNT
MENDONÇA, Berenice Bilharinho de et al. Female pseudohermaphroditism caused by a novel homozygous missense mutation of the GR gene. The Journal of Clinical Endocrinology & Metabolism, v. 87, n. 4, p. 1805-1809, 2002Tradução . . Acesso em: 19 abr. 2024. -
APA
Mendonça, B. B. de, Leite, M. V., Castro, M. de, Kino, T., Elias, L. L. K., Bachega, T. A. S., et al. (2002). Female pseudohermaphroditism caused by a novel homozygous missense mutation of the GR gene. The Journal of Clinical Endocrinology & Metabolism, 87( 4), 1805-1809. -
NLM
Mendonça BB de, Leite MV, Castro M de, Kino T, Elias LLK, Bachega TAS, Arnhold IJP, Chrousos GP, Latronico AC. Female pseudohermaphroditism caused by a novel homozygous missense mutation of the GR gene. The Journal of Clinical Endocrinology & Metabolism. 2002 ; 87( 4): 1805-1809.[citado 2024 abr. 19 ] -
Vancouver
Mendonça BB de, Leite MV, Castro M de, Kino T, Elias LLK, Bachega TAS, Arnhold IJP, Chrousos GP, Latronico AC. Female pseudohermaphroditism caused by a novel homozygous missense mutation of the GR gene. The Journal of Clinical Endocrinology & Metabolism. 2002 ; 87( 4): 1805-1809.[citado 2024 abr. 19 ] - Insuficiência adrenal primária de causa genética
- Etiopatogênese molecular dos tumores corticotróficos
- Bases moleculares da hiperplasia adrenal congênita
- Sensibilidade aos glicocorticóides (GC) in vivo e in vitro em indivíduos normais
- Glucocorticoid sensitivy in healthy individuals: in vitro and in vivo studies
- Basal plasma cortisol as a predictive value to determine secondary adrenal insuficiency
- Cerebral midline developmental anomalies: endocrine, neuroradiographic and ophthalmological features
- Variable ACTH-stimulated 17-Hydroxyprogesterone values in 21-hydroxylase deficiency carriers are not related to the different CYP21 gene mutations
- Absense of duplication on DAX1 gene in patients with 46,XY sex reversal
- Crescimento linear e estatura final em crianças com tumores adrenais predominantemente virilizantes
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas