Book syndrome: familial case report of a rare ectodermal dysplasia with learning disorders (2017)
Source: Resumos. Conference titles: Congresso Brasileiro de Genética Médica. Unidades: FORP, FMRP
Subjects: GENÉTICA MÉDICA, DISPLASIA ECTODÉRMICA, HERANÇA GENÉTICA
ABNT
CAVALCANTI, Thereza Taylanne Souza Loureiro et al. Book syndrome: familial case report of a rare ectodermal dysplasia with learning disorders. 2017, Anais.. Bento Gonçalves: SBGM, 2017. Disponível em: http://www.sbgm.org.br/imagens/conteudo/files/ANAIS.compressed.pdf. Acesso em: 07 out. 2024.APA
Cavalcanti, T. T. S. L., Maia, R. E., Torres, C. P., Huber, J., & Ramos, E. S. (2017). Book syndrome: familial case report of a rare ectodermal dysplasia with learning disorders. In Resumos. Bento Gonçalves: SBGM. Recuperado de http://www.sbgm.org.br/imagens/conteudo/files/ANAIS.compressed.pdfNLM
Cavalcanti TTSL, Maia RE, Torres CP, Huber J, Ramos ES. Book syndrome: familial case report of a rare ectodermal dysplasia with learning disorders [Internet]. Resumos. 2017 ;[citado 2024 out. 07 ] Available from: http://www.sbgm.org.br/imagens/conteudo/files/ANAIS.compressed.pdfVancouver
Cavalcanti TTSL, Maia RE, Torres CP, Huber J, Ramos ES. Book syndrome: familial case report of a rare ectodermal dysplasia with learning disorders [Internet]. Resumos. 2017 ;[citado 2024 out. 07 ] Available from: http://www.sbgm.org.br/imagens/conteudo/files/ANAIS.compressed.pdf