Loss-of-function mutations in a gene cause central precocius puberty (2013)
- Authors:
- Abreu, Ana Paula
- Dauber, Andrew
- Macedo, Delaine Bulcão
- Noel, Sekoni D.
- Brito, Vinicius Nahime
- Gill, John C.
- Cukier, Priscilla
- Thompson, Ian
- Navarro, Victor M.
- Gagliardi, Priscila C.
- Rodrigues, Tânia M.
- Kochi, Cristiane
- Longui, Carlos A.
- Beckers, Dominique
- Zegher, Francis de
- Montenegro, Luciana R.
- Mendonça, Berenice Bilharinho de
- Carroll, Rona S.
- Hirschhorn, Joel N.
- Xavier, Ana Claudia Latronico
- Kaiser, Ursula B.
- USP affiliated authors: XAVIER, ANA CLAUDIA LATRÔNICO - FM ; MENDONÇA, BERENICE BILHARINHO DE - FM ; MONTENEGRO, LUCIANA RIBEIRO - FM
- Unidade: FM
- Subjects: PUBERDADE PRECOCE; TRANSTORNOS DO CRESCIMENTO; ENDOCRINOPATIAS
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Hormone Research in Paediatrics
- ISSN: 1663-2818
- Volume/Número/Paginação/Ano: v. 80, suppl. 1, p. 35, res. FC4-138, 2013
- Conference titles: European Society for Paediatric Endocrinology (ESPE)/ Joint Meeting
-
ABNT
ABREU, Ana Paula et al. Loss-of-function mutations in a gene cause central precocius puberty. Hormone Research in Paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 21 maio 2024. , 2013 -
APA
Abreu, A. P., Dauber, A., Macedo, D. B., Noel, S. D., Brito, V. N., Gill, J. C., et al. (2013). Loss-of-function mutations in a gene cause central precocius puberty. Hormone Research in Paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. -
NLM
Abreu AP, Dauber A, Macedo DB, Noel SD, Brito VN, Gill JC, Cukier P, Thompson I, Navarro VM, Gagliardi PC, Rodrigues TM, Kochi C, Longui CA, Beckers D, Zegher F de, Montenegro LR, Mendonça BB de, Carroll RS, Hirschhorn JN, Xavier ACL, Kaiser UB. Loss-of-function mutations in a gene cause central precocius puberty. Hormone Research in Paediatrics. 2013 ; 80 35.[citado 2024 maio 21 ] -
Vancouver
Abreu AP, Dauber A, Macedo DB, Noel SD, Brito VN, Gill JC, Cukier P, Thompson I, Navarro VM, Gagliardi PC, Rodrigues TM, Kochi C, Longui CA, Beckers D, Zegher F de, Montenegro LR, Mendonça BB de, Carroll RS, Hirschhorn JN, Xavier ACL, Kaiser UB. Loss-of-function mutations in a gene cause central precocius puberty. Hormone Research in Paediatrics. 2013 ; 80 35.[citado 2024 maio 21 ] - Paternally inherited DLK1 deletion as novel cause of familial central precocious puberty
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