MID1 gene variations in a Brazilian cohort with cleft lip with or without palate and ocular hypertelorism: implication for diagnosis (2022)
- Autores:
- Zechi-Ceide, Roseli Maria
- Kokitsu-Nakata, Nancy Mizue
- Alvarez, Camila Wenceslau
- Migliore, Chiara
- Rafacho, Marina Bigeli
- Siemann, Maria Eugênia
- Candido-Souza, Rosana Maria
- Vendramini-Pittoli, Siulan
- Tonello, Cristiano
- Maximino, Luciana Paula
- Meroni, Germana
- Guion-Almeida, Maria Leine
- Opitz, John M.
- Richieri-Costa, Antonio
- Autores USP: CEIDE, ROSELI MARIA ZECHI - HRAC ; NAKATA, NANCY MIZUE KOKITSU - HRAC ; ALVAREZ, CAMILA WENCESLAU - HRAC ; PITTOLI, SIULAN VENDRAMINI PAULOVICH - HRAC ; TONELLO, CRISTIANO - FOB ; MAXIMINO, LUCIANA PAULA - FOB ; COSTA, ANTONIO RICHIERI DA - HRACF ; SOUZA, ROSANA MARIA CANDIDO DE - HRACF
- Unidades: HRAC; FOB; HRACF
- Assuntos: FISSURA LÁBIOPALATINA; HIPERTELORISMO; TRIAGEM; GENÉTICA
- Idioma: Inglês
- Imprenta:
- Fonte:
- Título do periódico: European Journal of Human Genetics
- ISSN: 1476-5438
- Volume/Número/Paginação/Ano: v. 30, supplement 1, p. 349-350, P11.079.A, 2022
- Nome do evento: European Society of Human Genetics
-
ABNT
ZECHI-CEIDE, Roseli Maria et al. MID1 gene variations in a Brazilian cohort with cleft lip with or without palate and ocular hypertelorism: implication for diagnosis. European Journal of Human Genetics. London: Hospital de Reabilitação de Anomalias Craniofaciais, Universidade de São Paulo. Disponível em: https://repositorio.usp.br/directbitstream/c7d85a5d-6ff4-412a-a203-f85d7c5b68b7/3089184.pdf. Acesso em: 23 abr. 2024. , 2022 -
APA
Zechi-Ceide, R. M., Kokitsu-Nakata, N. M., Alvarez, C. W., Migliore, C., Rafacho, M. B., Siemann, M. E., et al. (2022). MID1 gene variations in a Brazilian cohort with cleft lip with or without palate and ocular hypertelorism: implication for diagnosis. European Journal of Human Genetics. London: Hospital de Reabilitação de Anomalias Craniofaciais, Universidade de São Paulo. Recuperado de https://repositorio.usp.br/directbitstream/c7d85a5d-6ff4-412a-a203-f85d7c5b68b7/3089184.pdf -
NLM
Zechi-Ceide RM, Kokitsu-Nakata NM, Alvarez CW, Migliore C, Rafacho MB, Siemann ME, Candido-Souza RM, Vendramini-Pittoli S, Tonello C, Maximino LP, Meroni G, Guion-Almeida ML, Opitz JM, Richieri-Costa A. MID1 gene variations in a Brazilian cohort with cleft lip with or without palate and ocular hypertelorism: implication for diagnosis [Internet]. European Journal of Human Genetics. 2022 ; 30 349-350.[citado 2024 abr. 23 ] Available from: https://repositorio.usp.br/directbitstream/c7d85a5d-6ff4-412a-a203-f85d7c5b68b7/3089184.pdf -
Vancouver
Zechi-Ceide RM, Kokitsu-Nakata NM, Alvarez CW, Migliore C, Rafacho MB, Siemann ME, Candido-Souza RM, Vendramini-Pittoli S, Tonello C, Maximino LP, Meroni G, Guion-Almeida ML, Opitz JM, Richieri-Costa A. MID1 gene variations in a Brazilian cohort with cleft lip with or without palate and ocular hypertelorism: implication for diagnosis [Internet]. European Journal of Human Genetics. 2022 ; 30 349-350.[citado 2024 abr. 23 ] Available from: https://repositorio.usp.br/directbitstream/c7d85a5d-6ff4-412a-a203-f85d7c5b68b7/3089184.pdf - Holoprosencephaly, orofacial cleft, and frontonaso-orbital encephaloceles: genetic evaluation of a possible new syndrome
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