Male pseudohermaphroditism (mph) due to isolated 17,20-lyase deficiency (1995)
- Authors:
- USP affiliated authors: WAJCHENBERG, BERNARDO LEO - FM ; NICOLAU, WILIAN - FM
- Unidade: FM
- Assunto: ENDOCRINOLOGIA
- Language: Inglês
- Imprenta:
- Publisher: Endocrine Society
- Publisher place: Rockville
- Date published: 1995
- Source:
- Título: Program and Abstracts
- Conference titles: Annual Meeting of the Endocrine Society
-
ABNT
MENDONÇA, B. B. et al. Male pseudohermaphroditism (mph) due to isolated 17,20-lyase deficiency. 1995, Anais.. Rockville: Endocrine Society, 1995. . Acesso em: 16 fev. 2026. -
APA
Mendonça, B. B., Arnhold, I. J. P., Pelegrinelli, A. C., Frade, E. C., Latronico, A. C., Lin, C. J., et al. (1995). Male pseudohermaphroditism (mph) due to isolated 17,20-lyase deficiency. In Program and Abstracts. Rockville: Endocrine Society. -
NLM
Mendonça BB, Arnhold IJP, Pelegrinelli AC, Frade EC, Latronico AC, Lin CJ, Marcondes JAM, Nicolau W, Bloise W, Wajchenberg BL. Male pseudohermaphroditism (mph) due to isolated 17,20-lyase deficiency. Program and Abstracts. 1995 ;[citado 2026 fev. 16 ] -
Vancouver
Mendonça BB, Arnhold IJP, Pelegrinelli AC, Frade EC, Latronico AC, Lin CJ, Marcondes JAM, Nicolau W, Bloise W, Wajchenberg BL. Male pseudohermaphroditism (mph) due to isolated 17,20-lyase deficiency. Program and Abstracts. 1995 ;[citado 2026 fev. 16 ] - Mutation in 3'BETA'oxysteroid dehydrogenase type iii associated with pseudohermaphroditism in males and premature pubarche or cryptic expression in females
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