Source: American journal of medical genetics part a. Unidade: FM
Subjects: CONVULSÕES, CONVULSOTERAPIA
ABNT
NOBREGA, Paulo Ribeiro et al. Mystery solved after 23 years: M syndrome is PIGT-associated multiple congenital anomalies-hypotonia-seizures syndrome 3. American journal of medical genetics part a, v. 188, n. 12, p. 3567-3568, 2022Tradução . . Disponível em: https://observatorio.fm.usp.br/handle/OPI/50568. Acesso em: 15 nov. 2024.APA
Nobrega, P. R., Castro, M. A. A., Paiva, A. R. B. de, & Kok, F. (2022). Mystery solved after 23 years: M syndrome is PIGT-associated multiple congenital anomalies-hypotonia-seizures syndrome 3. American journal of medical genetics part a, 188( 12), 3567-3568. doi:10.1002/ajmg.a.62977NLM
Nobrega PR, Castro MAA, Paiva ARB de, Kok F. Mystery solved after 23 years: M syndrome is PIGT-associated multiple congenital anomalies-hypotonia-seizures syndrome 3 [Internet]. American journal of medical genetics part a. 2022 ; 188( 12): 3567-3568.[citado 2024 nov. 15 ] Available from: https://observatorio.fm.usp.br/handle/OPI/50568Vancouver
Nobrega PR, Castro MAA, Paiva ARB de, Kok F. Mystery solved after 23 years: M syndrome is PIGT-associated multiple congenital anomalies-hypotonia-seizures syndrome 3 [Internet]. American journal of medical genetics part a. 2022 ; 188( 12): 3567-3568.[citado 2024 nov. 15 ] Available from: https://observatorio.fm.usp.br/handle/OPI/50568