Phenotype–Genotype Correlations in Patients with Inactivating Gonadotropin Hormone Receptor Mutations (2012)
- Authors:
- USP affiliated authors: XAVIER, ANA CLAUDIA LATRÔNICO - FM ; MENDONÇA, BERENICE BILHARINHO DE - FM
- Unidade: FM
- Subjects: GENÓTIPOS; MUTAÇÃO GENÉTICA; FENÓTIPOS; HIPOGONADISMO; 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-618, 2012
- Conference titles: ENDO 2012: The Endocrine Society's 94th Annual Meeting & Expo
-
ABNT
BENEDUZZI, Daiane et al. Phenotype–Genotype Correlations in Patients with Inactivating Gonadotropin Hormone Receptor Mutations. Endocrine Reviews, v. 33, 2012Tradução . . Disponível em: http://edrv.endojournals.org/cgi/content/meeting_abstract/33/03_MeetingAbstracts/SUN-618. Acesso em: 11 mar. 2026. -
APA
Beneduzzi, D., Costa, E. M. F., Silveira, L., Trarbach, E., Abreu, A. P., Porto, A. L., et al. (2012). Phenotype–Genotype Correlations in Patients with Inactivating Gonadotropin Hormone Receptor Mutations. Endocrine Reviews, 33. Recuperado de http://edrv.endojournals.org/cgi/content/meeting_abstract/33/03_MeetingAbstracts/SUN-618 -
NLM
Beneduzzi D, Costa EMF, Silveira L, Trarbach E, Abreu AP, Porto AL, Latronico AC, Mendonca BB. Phenotype–Genotype Correlations in Patients with Inactivating Gonadotropin Hormone Receptor Mutations [Internet]. Endocrine Reviews. 2012 ; 33[citado 2026 mar. 11 ] Available from: http://edrv.endojournals.org/cgi/content/meeting_abstract/33/03_MeetingAbstracts/SUN-618 -
Vancouver
Beneduzzi D, Costa EMF, Silveira L, Trarbach E, Abreu AP, Porto AL, Latronico AC, Mendonca BB. Phenotype–Genotype Correlations in Patients with Inactivating Gonadotropin Hormone Receptor Mutations [Internet]. Endocrine Reviews. 2012 ; 33[citado 2026 mar. 11 ] Available from: http://edrv.endojournals.org/cgi/content/meeting_abstract/33/03_MeetingAbstracts/SUN-618 - Fatores determinantes da estatura final normal em meninas com puberdade precoce dependente de gonadotrofinas tratadas com análogos de GnRII depot
- Análise dos valares de LH 2 horas após acetato de leuprolide depot na monitorização do tratamento da puberdade precoce dependente de gonadotrofinas
- Frequency of molecular diagnosis in brazilian patients with 46,XY disorders of sexual development (DSD)
- Genetic analysis of thyroid transcription factor1 (TTF-1) gene in patients with central pubertal disorders
- Mutation in PTPN11 gene are a common cause of noonan syndrome (NS) but are not a selective IGF-1 receptor kinase inhibitor (NVP-AEW541) suppresses proliferation of the human adrenocortical cancer cell line NCI H295 due to apoptosis induction
- XAF1 as a modifier of p53 function and cancer susceptibility
- Localization of Occult Adrenal Tissue with Cosyntropin-Stimulated 18F-FDG-PET/CT in a Patient with Metachronous Adrenocortical Tumor Who Presented with Persistently Elevated DHEAS after Bilateral Adrenalectomy
- A novel missense variant in the Necdin gene in a male patient with kallmann syndrome
- Molecular analysis of the neuropeptide Y1 receptor gene in human idiopathic gonadotropin-dependent precocious puberty and isolated hypogonadotropic hypogonadism
- Paternally Inherited DLK1 Deletion Associated With Familial Central Precocious Puberty
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
