Insights from the genetic characterization of central precocious puberty associated with multiple anomalies (2021)
- Authors:
- Canton, Ana Pinheiro Machado
- Krepischi, Ana Cristina Victorino
- Montenegro, Luciana Ribeiro
- Costa, Silvia
- Rosenberg, Carla
- Steunou, Virginie
- Sobrier, Marie-Laure
- Santana, Lucas
- Honjo, Rachel Sayuri
- Kim, Chong Ae
- Francis de Zegher
- Idkowiak, Jan
- Gilligan, Lorna C
- Arlt, Wiebke
- Funari, Mariana Ferreira de Assis
- Jorge, Alexander Augusto de Lima
- Mendonca, Berenice Bilharinho de
- Netchine, Irène
- Brito, Vinicius Nahime de
- Latronico, Ana Claudia
- Canton, Ana Pinheiro Machado
- USP affiliated authors: COSTA, SILVIA SOUZA DA - IB ; ROSENBERG, CARLA - IB ; KIM, CHONG AE - FM ; MENDONÇA, BERENICE BILHARINHO DE - FM ; BRITO, VINICIUS NAHIME DE - FM ; XAVIER, ANA CLAUDIA LATRÔNICO - FM ; KREPISCHI, ANA CRISTINA VICTORINO - IB ; MONTENEGRO, LUCIANA RIBEIRO - FM ; SANTANA, LUCAS SANTOS DE - FM ; KAWAHIRA, RACHEL SAYURI HONJO - FM ; FUNARI, MARIANA FERREIRA DE ASSIS - FM ; JORGE, ALEXANDER AUGUSTO DE LIMA - FM ; CANTON, ANA PINHEIRO MACHADO - FM
- Unidades: IB; FM
- DOI: 10.1093/humrep/deaa306
- Subjects: PUBERDADE PRECOCE; GENÉTICA; DOENÇAS GENÉTICAS; ANORMALIDADES CROMOSSÔMICAS
- Agências de fomento:
- Language: Inglês
- Imprenta:
- Publisher place: Grimbergen
- Date published: 2021
- Source:
- Título: Human Reproduction
- ISSN: 0268-1161
- Volume/Número/Paginação/Ano: v. 36, n. 2, p. 506-518, 2021
- Este periódico é de assinatura
- Este artigo é de acesso aberto
- URL de acesso aberto
- Cor do Acesso Aberto: bronze
-
ABNT
CANTON, Ana Pinheiro Machado et al. Insights from the genetic characterization of central precocious puberty associated with multiple anomalies. Human Reproduction, v. 36, n. 2, p. 506-518, 2021Tradução . . Disponível em: https://doi.org/10.1093/humrep/deaa306. Acesso em: 11 jan. 2026. -
APA
Canton, A. P. M., Krepischi, A. C. V., Montenegro, L. R., Costa, S., Rosenberg, C., Steunou, V., et al. (2021). Insights from the genetic characterization of central precocious puberty associated with multiple anomalies. Human Reproduction, 36( 2), 506-518. doi:10.1093/humrep/deaa306 -
NLM
Canton APM, Krepischi ACV, Montenegro LR, Costa S, Rosenberg C, Steunou V, Sobrier M-L, Santana L, Honjo RS, Kim CA, Francis de Zegher, Idkowiak J, Gilligan LC, Arlt W, Funari MF de A, Jorge AA de L, Mendonca BB de, Netchine I, Brito VN de, Latronico AC. Insights from the genetic characterization of central precocious puberty associated with multiple anomalies [Internet]. Human Reproduction. 2021 ; 36( 2): 506-518.[citado 2026 jan. 11 ] Available from: https://doi.org/10.1093/humrep/deaa306 -
Vancouver
Canton APM, Krepischi ACV, Montenegro LR, Costa S, Rosenberg C, Steunou V, Sobrier M-L, Santana L, Honjo RS, Kim CA, Francis de Zegher, Idkowiak J, Gilligan LC, Arlt W, Funari MF de A, Jorge AA de L, Mendonca BB de, Netchine I, Brito VN de, Latronico AC. Insights from the genetic characterization of central precocious puberty associated with multiple anomalies [Internet]. Human Reproduction. 2021 ; 36( 2): 506-518.[citado 2026 jan. 11 ] Available from: https://doi.org/10.1093/humrep/deaa306 - Pathogenic copy number variants in patients with congenital hypopituitarism associated with complex phenotypes
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- Clinical and Genetic Characterization of Familial Central Precocious Puberty
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- Molecular and cellular basis of hyperassembly and protein aggregation driven by a rare pathogenic mutation in DDX3X
- Paternally inherited DLK1 deletion as novel cause of familial central precocious puberty
- Central Precocious Puberty Caused by a Heterozygous Deletion in the MKRN3 Promoter Region
- Loss-of-function mutations in a gene cause central precocius puberty
- High Frequency of MKRN3 Mutations in Male Central Precocious Puberty Previously Classified as Idiopathic
- Novel mutations (P.G6R and P.R511W) in IGF1R gene in children born small for gestational age (SGA) without catch-up growth
Informações sobre o DOI: 10.1093/humrep/deaa306 (Fonte: oaDOI API)
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