Fonte: Human Mutation. Unidade: IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SPLENDORE, Alessandra et al. High mutation detection rate in TCOF1 among treacher Collins Syndrome patients reveals clustering of mutation and 16 novel pathogenic changes. Human Mutation, v. 16, p. 315-322, 2000Tradução . . Disponível em: https://doi.org/10.1002/1098-1004(200010)16:4%3C315::aid-humu4%3E3.0.co;2-h. Acesso em: 27 set. 2024.APA
Splendore, A., Silva, E. O. da, Alonso, L. G., Richieri-Costa, A., Alonso, N., Rosa, A., et al. (2000). High mutation detection rate in TCOF1 among treacher Collins Syndrome patients reveals clustering of mutation and 16 novel pathogenic changes. Human Mutation, 16, 315-322. doi:10.1002/1098-1004(200010)16:4%3C315::aid-humu4%3E3.0.co;2-hNLM
Splendore A, Silva EO da, Alonso LG, Richieri-Costa A, Alonso N, Rosa A, Carakushansky G, Cavalcanti DP, Brunoni D, Passos-Bueno MR. High mutation detection rate in TCOF1 among treacher Collins Syndrome patients reveals clustering of mutation and 16 novel pathogenic changes [Internet]. Human Mutation. 2000 ; 16 315-322.[citado 2024 set. 27 ] Available from: https://doi.org/10.1002/1098-1004(200010)16:4%3C315::aid-humu4%3E3.0.co;2-hVancouver
Splendore A, Silva EO da, Alonso LG, Richieri-Costa A, Alonso N, Rosa A, Carakushansky G, Cavalcanti DP, Brunoni D, Passos-Bueno MR. High mutation detection rate in TCOF1 among treacher Collins Syndrome patients reveals clustering of mutation and 16 novel pathogenic changes [Internet]. Human Mutation. 2000 ; 16 315-322.[citado 2024 set. 27 ] Available from: https://doi.org/10.1002/1098-1004(200010)16:4%3C315::aid-humu4%3E3.0.co;2-h