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Filtros : "MONTENEGRO, LUCIANA RIBEIRO" "2017" Limpar

Filtros

Trabalho de evento-resumo periodico
Paternally inherited DLK1 deletion as novel cause of familial central precocious puberty (2017)
Dauber, Andrew; Montenegro, Luciana Ribeiro; Mendonça, Berenice Bilharinho de; Xavier, Ana Claudia Latronico
Source: Hormone research in paediatrics. Conference titles: Joint meeting of paediatric endocrinology. Unidade: FM
Subjects: PUBERDADE PRECOCE, MUTAÇÃO GENÉTICA, ANORMALIDADES CROMOSSÔMICAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
DAUBER, Andrew et al. Paternally inherited DLK1 deletion as novel cause of familial central precocious puberty. Hormone research in paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 09 nov. 2024. , 2017
APA
Dauber, A., Montenegro, L. R., Mendonça, B. B. de, & Xavier, A. C. L. (2017). Paternally inherited DLK1 deletion as novel cause of familial central precocious puberty. Hormone research in paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo.
NLM
Dauber A, Montenegro LR, Mendonça BB de, Xavier ACL. Paternally inherited DLK1 deletion as novel cause of familial central precocious puberty. Hormone research in paediatrics. 2017 ; 88[citado 2024 nov. 09 ]
Vancouver
Dauber A, Montenegro LR, Mendonça BB de, Xavier ACL. Paternally inherited DLK1 deletion as novel cause of familial central precocious puberty. Hormone research in paediatrics. 2017 ; 88[citado 2024 nov. 09 ]
Artigo de periodico
High Frequency of MKRN3 Mutations in Male Central Precocious Puberty Previously Classified as Idiopathic (2017)
Bessa, Danielle S.; Montenegro, Luciana Ribeiro; Mendonça, Berenice Bilharinho de; Xavier, Ana Claudia Latronico
Source: Neuroendocrinology. Unidade: FM
Subjects: MUTAÇÃO GENÉTICA, PUBERDADE PRECOCE, DOENÇAS HEREDITÁRIAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BESSA, Danielle S. et al. High Frequency of MKRN3 Mutations in Male Central Precocious Puberty Previously Classified as Idiopathic. Neuroendocrinology, v. 105, n. 1, p. 17-25, 2017Tradução . . Disponível em: https://doi.org/10.1159/000446963. Acesso em: 09 nov. 2024.
APA
Bessa, D. S., Montenegro, L. R., Mendonça, B. B. de, & Xavier, A. C. L. (2017). High Frequency of MKRN3 Mutations in Male Central Precocious Puberty Previously Classified as Idiopathic. Neuroendocrinology, 105( 1), 17-25. doi:10.1159/000446963
NLM
Bessa DS, Montenegro LR, Mendonça BB de, Xavier ACL. High Frequency of MKRN3 Mutations in Male Central Precocious Puberty Previously Classified as Idiopathic [Internet]. Neuroendocrinology. 2017 ; 105( 1): 17-25.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1159/000446963
Vancouver
Bessa DS, Montenegro LR, Mendonça BB de, Xavier ACL. High Frequency of MKRN3 Mutations in Male Central Precocious Puberty Previously Classified as Idiopathic [Internet]. Neuroendocrinology. 2017 ; 105( 1): 17-25.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1159/000446963

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