A new mutation in GHR gene located in WSXWS-like motif in a child with laron syndrome (2002)
- Authors:
- USP affiliated authors: MENDONCA, BERENICE BILHARINHO DE - FM ; ARNHOLD, IVO JORGE PRADO - FM
- Unidade: FM
- Assunto: ENDOCRINOLOGIA
- Language: Inglês
- Imprenta:
- Publisher place: San Francisco
- Date published: 2002
- Source:
- Título do periódico: Resumos
- Conference titles: Annual Metting the Endrocrine Society's
-
ABNT
JORGE, Alexander A. L. et al. A new mutation in GHR gene located in WSXWS-like motif in a child with laron syndrome. 2002, Anais.. San Francisco: Faculdade de Medicina, Universidade de São Paulo, 2002. . Acesso em: 24 abr. 2024. -
APA
Jorge, A. A. L., Lin, C. J., Souza, S. C. A. L., Arnhold, I. J. P., & Mendonça, B. B. de. (2002). A new mutation in GHR gene located in WSXWS-like motif in a child with laron syndrome. In Resumos. San Francisco: Faculdade de Medicina, Universidade de São Paulo. -
NLM
Jorge AAL, Lin CJ, Souza SCAL, Arnhold IJP, Mendonça BB de. A new mutation in GHR gene located in WSXWS-like motif in a child with laron syndrome. Resumos. 2002 ;[citado 2024 abr. 24 ] -
Vancouver
Jorge AAL, Lin CJ, Souza SCAL, Arnhold IJP, Mendonça BB de. A new mutation in GHR gene located in WSXWS-like motif in a child with laron syndrome. Resumos. 2002 ;[citado 2024 abr. 24 ] - Variable ACTH-stimulated 17-Hydroxyprogesterone values in 21-hydroxylase deficiency carriers are not related to the different CYP21 gene mutations
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