Paternally Inherited DLK1 Deletion Associated With Familial Central Precocious Puberty (2017)
- Authors:
- Dauber, Andrew
- Cunha-Silva, Marina
- Macedo, Delanie B.
- Brito, Vinicius N.
- Abreu, Ana Paula
- Roberts, Stephanie A.
- Montenegro, Luciana R.
- Andrew, Melissa
- Kirby, Andrew
- Weirauch, Matthew T.
- Labilloy, Guillaume
- Bessa, Danielle S.
- Carroll, Rona S.
- Jacobs, Dakota C.
- Chappell, Patrick E.
- Mendonca, Berenice B.
- Haig, David
- Kaiser, Ursula B.
- Latronico, Ana Claudia
- USP affiliated authors: XAVIER, ANA CLAUDIA LATRÔNICO - FM ; MENDONÇA, BERENICE BILHARINHO DE - FM
- Unidade: FM
- DOI: 10.1210/jc.2016-3677
- Subjects: PUBERDADE PRECOCE; REAÇÃO EM CADEIA POR POLIMERASE; HIPOTÁLAMO; MUTAÇÃO GENÉTICA
- Language: Inglês
- Imprenta:
- Publisher place: Springfield
- Date published: 2017
- Source:
- Título do periódico: Journal of clinical endocrinology and metabolism
- ISSN: 0021-972X
- Volume/Número/Paginação/Ano: v. 102, n. 5, p. 1557-1567, 2017
- Este periódico é de assinatura
- Este artigo é de acesso aberto
- URL de acesso aberto
- Cor do Acesso Aberto: bronze
-
ABNT
DAUBER, Andrew et al. Paternally Inherited DLK1 Deletion Associated With Familial Central Precocious Puberty. Journal of clinical endocrinology and metabolism, v. 102, n. 5, p. 1557-1567, 2017Tradução . . Disponível em: https://doi.org/10.1210/jc.2016-3677. Acesso em: 19 abr. 2024. -
APA
Dauber, A., Cunha-Silva, M., Macedo, D. B., Brito, V. N., Abreu, A. P., Roberts, S. A., et al. (2017). Paternally Inherited DLK1 Deletion Associated With Familial Central Precocious Puberty. Journal of clinical endocrinology and metabolism, 102( 5), 1557-1567. doi:10.1210/jc.2016-3677 -
NLM
Dauber A, Cunha-Silva M, Macedo DB, Brito VN, Abreu AP, Roberts SA, Montenegro LR, Andrew M, Kirby A, Weirauch MT, Labilloy G, Bessa DS, Carroll RS, Jacobs DC, Chappell PE, Mendonca BB, Haig D, Kaiser UB, Latronico AC. Paternally Inherited DLK1 Deletion Associated With Familial Central Precocious Puberty [Internet]. Journal of clinical endocrinology and metabolism. 2017 ; 102( 5): 1557-1567.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1210/jc.2016-3677 -
Vancouver
Dauber A, Cunha-Silva M, Macedo DB, Brito VN, Abreu AP, Roberts SA, Montenegro LR, Andrew M, Kirby A, Weirauch MT, Labilloy G, Bessa DS, Carroll RS, Jacobs DC, Chappell PE, Mendonca BB, Haig D, Kaiser UB, Latronico AC. Paternally Inherited DLK1 Deletion Associated With Familial Central Precocious Puberty [Internet]. Journal of clinical endocrinology and metabolism. 2017 ; 102( 5): 1557-1567.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1210/jc.2016-3677 - Update on the etiology, diagnosis and therapeutic management of sexual precocity
- A novel missense variant in the Necdin gene in a male patient with kallmann syndrome
- 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
- Central Precocious Puberty Caused by Mutations in the Imprinted Gene MKRN3
- Frequency of molecular diagnosis in brazilian patients with 46,XY disorders of sexual development (DSD)
- Analysis of LH determination 2 hours after depot leuprolide acetate in monitoring gonadotropin-dependent precocious puberty treatment
- Two Kiss1 mutations associated with gonadotropin-dependent precocious puberty
- Anthropometric, metabolic and reproductive outcome of patients with central precocious puberty due to hypothalamic hamartoma in adult life
- Puberdade precoce central
- Methylome profiling of healthy and central precocious puberty girls
Informações sobre o DOI: 10.1210/jc.2016-3677 (Fonte: oaDOI API)
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
