The unusually high incidence of germline Arg337His mutation in the p53 tumor suppressor gene among brazilian with adrenocortical tumors can be attributed to founder effect (2004)
- Authors:
- USP affiliated author: MENDONÇA, BERENICE BILHARINHO DE - FM
- School: FM
- Subjects: BIOMARCADORES; MUTAÇÃO GENÉTICA; POLIMORFISMO; GENES SUPRESSORES DE TUMOR; BRASILEIROS
- Language: Inglês
- Imprenta:
- Publisher: International Society of Endocrinology
- Place of publication: Lisboa
- Date published: 2004
- Source:
- Título do periódico: Program and Abstracts
- Conference title: International Congress of Endocrinology
-
ABNT
PINTO, E. M. et al. The unusually high incidence of germline Arg337His mutation in the p53 tumor suppressor gene among brazilian with adrenocortical tumors can be attributed to founder effect. 2004, Anais.. Lisboa: International Society of Endocrinology, 2004. . Acesso em: 01 jul. 2022. -
APA
Pinto, E. M., Billerbeck, A. E., Mendonca, B. B., & Latronico, A. C. (2004). The unusually high incidence of germline Arg337His mutation in the p53 tumor suppressor gene among brazilian with adrenocortical tumors can be attributed to founder effect. In Program and Abstracts. Lisboa: International Society of Endocrinology. -
NLM
Pinto EM, Billerbeck AE, Mendonca BB, Latronico AC. The unusually high incidence of germline Arg337His mutation in the p53 tumor suppressor gene among brazilian with adrenocortical tumors can be attributed to founder effect. Program and Abstracts. 2004 ;[citado 2022 jul. 01 ] -
Vancouver
Pinto EM, Billerbeck AE, Mendonca BB, Latronico AC. The unusually high incidence of germline Arg337His mutation in the p53 tumor suppressor gene among brazilian with adrenocortical tumors can be attributed to founder effect. Program and Abstracts. 2004 ;[citado 2022 jul. 01 ] - Molecular analysis of SRY gene in Brazilian 46,XX sex reversed patients: absense of SRY sequence in gonadal tissue
- Crescimento linear e estatura final em crianças com tumores adrenais predominantemente virilizantes
- Clinical, hormonal, behavioral, and genetic characteristics of androgen insensitibity syndrome in a brazilian cohort: five novel mutations in the androgen receptor gene
- Heterogeneidade clínica e molecular do hipogonadismo hipogonadotrófico (HH): importância da avaliação do sistema olfatório no diagnóstico diferencial
- Absense of duplication on DAX1 gene in patients with 46,XY sex reversal
- Absense of inactivating mutations and deletions of DAX1 gene in SRY negative 46,XX sex-reversed patients
- Variable ACTH-stimulated 17-Hydroxyprogesterone values in 21-hydroxylase deficiency carriers are not related to the different CYP21 gene mutations
- Microconversão no promotor do gene CYP21A2 envolvendo os sítios de ligação dos fatores de transcrição Sp1 e ASP: nova etiologia molecular da deficiência de 21-hidroxilase (21OHD)
- Nova etiologia da deficiência da 21OH: microconversão nos sítios de liga dos fatores de transcrição Sp1 e ASP no promotor do gene CYP21A2
- Amenorréia primária causada por uma deficiência seletiva de FSH a uma mutação inativadora no gene da subunidade beta do FSH (FSH beta)
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
