47,XXY Klinefelter Syndrome Associated with Partial Androgen Insensitivity Phenotype Conferred by a Complete Inactivating Mutation in the Androgen Receptor Gene (2012)
- Authors:
- Autor USP: MENDONÇA, BERENICE BILHARINHO DE - FM
- Unidade: FM
- Subjects: ANDROGINIA; GENÓTIPOS; AMENORREIA; MUTAÇÃO GENÉTICA; TEXTOSTERONA (ANÁLISE); RESUMOS (EVENTOS)
- Language: Inglês
- Imprenta:
- Publisher place: Chevy Chase
- Date published: 2012
- Source:
- Título: Endocrine Reviews
- ISSN: 0163-769X
- Volume/Número/Paginação/Ano: v. 33, 03_meetingAbstracts, Res. SUN-77, 2012
- Conference titles: ENDO 2012: The Endocrine Society's 94th Annual Meeting & Expo
-
ABNT
CARVALHO, Luciane C. de et al. 47,XXY Klinefelter Syndrome Associated with Partial Androgen Insensitivity Phenotype Conferred by a Complete Inactivating Mutation in the Androgen Receptor Gene. Endocrine Reviews, v. 33, 2012Tradução . . Disponível em: http://edrv.endojournals.org/cgi/content/meeting_abstract/33/03_MeetingAbstracts/SUN-77. Acesso em: 27 dez. 2025. -
APA
Carvalho, L. C. de, Carvalho, L. C. de, Feitosa, A. C. R., Rodrigues, A. de S., Nishi, M. Y., Silva, R. B., et al. (2012). 47,XXY Klinefelter Syndrome Associated with Partial Androgen Insensitivity Phenotype Conferred by a Complete Inactivating Mutation in the Androgen Receptor Gene. Endocrine Reviews, 33. Recuperado de http://edrv.endojournals.org/cgi/content/meeting_abstract/33/03_MeetingAbstracts/SUN-77 -
NLM
Carvalho LC de, Carvalho LC de, Feitosa ACR, Rodrigues A de S, Nishi MY, Silva RB, Costa EMF, Domenice S, Mendonca BB. 47,XXY Klinefelter Syndrome Associated with Partial Androgen Insensitivity Phenotype Conferred by a Complete Inactivating Mutation in the Androgen Receptor Gene [Internet]. Endocrine Reviews. 2012 ; 33[citado 2025 dez. 27 ] Available from: http://edrv.endojournals.org/cgi/content/meeting_abstract/33/03_MeetingAbstracts/SUN-77 -
Vancouver
Carvalho LC de, Carvalho LC de, Feitosa ACR, Rodrigues A de S, Nishi MY, Silva RB, Costa EMF, Domenice S, Mendonca BB. 47,XXY Klinefelter Syndrome Associated with Partial Androgen Insensitivity Phenotype Conferred by a Complete Inactivating Mutation in the Androgen Receptor Gene [Internet]. Endocrine Reviews. 2012 ; 33[citado 2025 dez. 27 ] Available from: http://edrv.endojournals.org/cgi/content/meeting_abstract/33/03_MeetingAbstracts/SUN-77 - Molecular analysis of SRY gene in Brazilian 46,XX sex reversed patients: absense of SRY sequence in gonadal tissue
- Clinical and molecular analysis of human reproductive disorders in brazilian patients
- Amenorréia primária causada por uma deficiência seletiva de FSH a uma mutação inativadora no gene da subunidade beta do FSH (FSH beta)
- Molecular analysis of two distinct candidate genes (GABRA1 and NPY-Y1) that could be implicated in the human puberty timing
- Nova etiologia da deficiência da 21OH: microconversão nos sítios de liga dos fatores de transcrição Sp1 e ASP no promotor do gene CYP21A2
- Clinical and molecular heterogeneity of hypogonadotropic hypogonadism (HH):: importance of olfactory system assessment in the differential diagnosis
- Reprodutive outcome of women with 21-Hydroxylase (21-OH) deficient non classic adrenal hyperplasia (NCAH):: a multicenter study
- Caracterização clínica e hormonal de pacientes portadores de deficiência hormonal hipofisária múltipla por mutação no gene PROP-1
- Ausência de haploinsuficiência do gene DAX1 em pacientes portadores de sexo 46,XX
- Valor da dosagem de gonadotrofinas pelo metodo imunofluorométrico ultrassensível no diagnóstico do hipogonadismo hipogonadotrófico (HH)
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas