A novel germiline mutation (6747_6748insG) of MEN1 Gene, in a patient with multiple endocrine neoplasia type 1 (2004)
- Autores:
- Autor USP: MENDONÇA, BERENICE BILHARINHO DE - FM
- Unidade: FM
- Assuntos: NEOPLASIA ENDÓCRINA MÚLTIPLA; MUTAÇÃO GENÉTICA; TIREOIDECTOMIA; HIPERTIREOIDISMO (COMPLICAÇÕES); METÁSTASE (COMPLICAÇÕES)
- Idioma: Inglês
- Imprenta:
- Editora: International Society of Endocrinology
- Local: Lisboa
- Data de publicação: 2004
- Fonte:
- Título do periódico: Program and Abstracts
- Nome do evento: International Congress of Endocrinology
-
ABNT
COSTA, M. H. S. et al. A novel germiline mutation (6747_6748insG) of MEN1 Gene, in a patient with multiple endocrine neoplasia type 1. 2004, Anais.. Lisboa: International Society of Endocrinology, 2004. . Acesso em: 19 abr. 2024. -
APA
Costa, M. H. S., Domenice, S., Pinto, E. M., Martin, R. M., Mimura, L. Y., Mendonca, B. B., & Fragoso, M. C. B. V. (2004). A novel germiline mutation (6747_6748insG) of MEN1 Gene, in a patient with multiple endocrine neoplasia type 1. In Program and Abstracts. Lisboa: International Society of Endocrinology. -
NLM
Costa MHS, Domenice S, Pinto EM, Martin RM, Mimura LY, Mendonca BB, Fragoso MCBV. A novel germiline mutation (6747_6748insG) of MEN1 Gene, in a patient with multiple endocrine neoplasia type 1. Program and Abstracts. 2004 ;[citado 2024 abr. 19 ] -
Vancouver
Costa MHS, Domenice S, Pinto EM, Martin RM, Mimura LY, Mendonca BB, Fragoso MCBV. A novel germiline mutation (6747_6748insG) of MEN1 Gene, in a patient with multiple endocrine neoplasia type 1. Program and Abstracts. 2004 ;[citado 2024 abr. 19 ] - Variable ACTH-stimulated 17-Hydroxyprogesterone values in 21-hydroxylase deficiency carriers are not related to the different CYP21 gene mutations
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