Autosomal recessive kallmann syndrome caused by mutations in the genes encoding prokineticin 2 and prokineticin receptor 2 (2008)
- Authors:
- USP affiliated authors: CASTRO, MARGARET DE - FMRP ; MENDONÇA, BERENICE BILHARINHO DE - FM
- Unidades: FMRP; FM
- Subjects: MUTAÇÃO GENÉTICA; GONADOTROFINAS
- Language: Inglês
- Imprenta:
- Publisher place: San Francisco
- Date published: 2008
- Source:
- Título: Program and Abstracts Book
- Conference titles: Annual Meeting of the Endocrine Society
-
ABNT
ABREU, A. P. et al. Autosomal recessive kallmann syndrome caused by mutations in the genes encoding prokineticin 2 and prokineticin receptor 2. 2008, Anais.. San Francisco: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, 2008. . Acesso em: 28 dez. 2025. -
APA
Abreu, A. P., Trarbach, E. B., Castro, M. de, Costa, E. M. F., Versiani, B., Guerra Júnior, G., et al. (2008). Autosomal recessive kallmann syndrome caused by mutations in the genes encoding prokineticin 2 and prokineticin receptor 2. In Program and Abstracts Book. San Francisco: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. -
NLM
Abreu AP, Trarbach EB, Castro M de, Costa EMF, Versiani B, Guerra Júnior G, Baptista MTM, Garmes HM, Mendonça BB de, Latronico AC. Autosomal recessive kallmann syndrome caused by mutations in the genes encoding prokineticin 2 and prokineticin receptor 2. Program and Abstracts Book. 2008 ;[citado 2025 dez. 28 ] -
Vancouver
Abreu AP, Trarbach EB, Castro M de, Costa EMF, Versiani B, Guerra Júnior G, Baptista MTM, Garmes HM, Mendonça BB de, Latronico AC. Autosomal recessive kallmann syndrome caused by mutations in the genes encoding prokineticin 2 and prokineticin receptor 2. Program and Abstracts Book. 2008 ;[citado 2025 dez. 28 ] - Two novel nonsense mutations of the fibroblast growth factor 8 in patients with congenital isolated hypogonadotropic hypogonadism
- Long-term treatment of familial male-limited precocious puberty (testotoxicosis) with cyproterone acetate or ketoconazole
- Long-term treatment of familial male-limited precocious puberty: Comparison between cyproterone and ketoconazole therapies
- Clinical and molecular analysis of TAC3 and TACR3 genes in Brazilian patients with isolated hypogonadotropic hypogonadism
- Hemizygous deletion of FGFR1 gene identified in a patient with congenital normosmic isolated hypogonadotropic hypogonadism by ligation-dependent probe amplification analysis
- Analysis of the promoter region of HESX1 in patients with combined pituitary hormone deficiency (CPHD) without mutations in the HESX1 coding sequence
- Novel mutations in CYP11B1 gene leading to 11 'beta'-hydroxylase deficiencey in brazilian patients
- Análise da região promotora do gene HESX1 em pacientes com deficiência hormonal hipofisária combinada (DHHC) sem mutações na região codoficadora do HESX1
- Inhibin alfa-subunit (INHA) gene and locus changes in paediatric adrenocortical tumours from TP53 R337H mutation heterozygote carriers
- Glucocorticoid receptor structure in ACTH-producing pituitary tumors
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
