Holoprosencephaly, orofacial cleft, and frontonaso-orbital encephaloceles: genetic evaluation of a possible new syndrome (2019)
- Authors:
- Richieri-Costa, Antonio
- Zechi-Ceide, Roseli Maria
- Souza, Rosana Maria Candido
- Monteiro, Rejane Alves de Carvalho
- Tonello, Cristiano
- Freitas, Mariana L. de
- Nakata, Nancy Mizue Kokitsu
- Pittoli, Siulan Vendramini Paulovich
- Mazzeu, Juliana F
- Overes, Madelief
- Ali-Amin, Roza
- van Slegtenhorst, Marjon
- Hoefsloot, Lies H
- Jehee, Fernanda S
- Richieri-Costa, Antonio
- USP affiliated authors: COSTA, ANTONIO RICHIERI DA - HRAC ; CEIDE, ROSELI MARIA ZECHI - HRAC ; TONELLO, CRISTIANO - HRAC ; NAKATA, NANCY MIZUE KOKITSU - HRAC ; PITTOLI, SIULAN VENDRAMINI PAULOVICH - HRAC ; SOUZA, ROSANA MARIA CANDIDO DE - HRACF
- Unidades: HRAC; HRACF
- DOI: 10.1002/ajmg.a.61305
- Subjects: GENÉTICA; HOLOPROSENCEFALIA; FISSURA LÁBIOPALATINA; ANORMALIDADES CRANIOFACIAIS
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: American Journal of Medical Genetics
- ISSN: 1552-4825
- Volume/Número/Paginação/Ano: v. 179A, n. 11, p. 2170-2177, Nov. 2019
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
RICHIERI-COSTA, Antonio et al. Holoprosencephaly, orofacial cleft, and frontonaso-orbital encephaloceles: genetic evaluation of a possible new syndrome. American Journal of Medical Genetics, v. No 2019, n. 11, p. 2170-2177, 2019Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.61305. Acesso em: 27 abr. 2024. -
APA
Richieri-Costa, A., Zechi-Ceide, R. M., Souza, R. M. C., Monteiro, R. A. de C., Tonello, C., Freitas, M. L. de, et al. (2019). Holoprosencephaly, orofacial cleft, and frontonaso-orbital encephaloceles: genetic evaluation of a possible new syndrome. American Journal of Medical Genetics, No 2019( 11), 2170-2177. doi:10.1002/ajmg.a.61305 -
NLM
Richieri-Costa A, Zechi-Ceide RM, Souza RMC, Monteiro RA de C, Tonello C, Freitas ML de, Nakata NMK, Pittoli SVP, Mazzeu JF, Overes M, Ali-Amin R, van Slegtenhorst M, Hoefsloot LH, Jehee FS. Holoprosencephaly, orofacial cleft, and frontonaso-orbital encephaloceles: genetic evaluation of a possible new syndrome [Internet]. American Journal of Medical Genetics. 2019 ; No 2019( 11): 2170-2177.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1002/ajmg.a.61305 -
Vancouver
Richieri-Costa A, Zechi-Ceide RM, Souza RMC, Monteiro RA de C, Tonello C, Freitas ML de, Nakata NMK, Pittoli SVP, Mazzeu JF, Overes M, Ali-Amin R, van Slegtenhorst M, Hoefsloot LH, Jehee FS. Holoprosencephaly, orofacial cleft, and frontonaso-orbital encephaloceles: genetic evaluation of a possible new syndrome [Internet]. American Journal of Medical Genetics. 2019 ; No 2019( 11): 2170-2177.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1002/ajmg.a.61305 - Microphthalmia, linear skin defects, callosal agenesis, and cleft palate in a patient with deletion at Xp22.3p22.2
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Informações sobre o DOI: 10.1002/ajmg.a.61305 (Fonte: oaDOI API)
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