A review of craniofacial disorders caused by spliceosomal defects (2015)
- Authors:
- USP affiliated authors: CEIDE, ROSELI MARIA ZECHI - HRAC ; BUENO, MARIA RITA DOS SANTOS E PASSOS - IB
- Unidades: HRAC; IB
- DOI: 10.1111/cge.12596
- Subjects: ANOMALIA CRANIOFACIAL; MALFORMAÇÕES
- Language: Inglês
- Imprenta:
- Source:
- Título: Clinical Genetics
- ISSN: 1399-0004
- Volume/Número/Paginação/Ano: p. on-line
- Este periódico é de acesso aberto
- Este artigo NÃO é de acesso aberto
-
ABNT
LEHALLEA, D. et al. A review of craniofacial disorders caused by spliceosomal defects. Clinical Genetics, p. on-line, 2015Tradução . . Disponível em: https://doi.org/10.1111/cge.12596. Acesso em: 14 fev. 2026. -
APA
Lehallea, D., Wieczorek, D., Zechi-Ceide, R. M., Passos-Bueno, M. R., Lyonnet, S., Amie, J., & Gordon, C. T. (2015). A review of craniofacial disorders caused by spliceosomal defects. Clinical Genetics, on-line. doi:10.1111/cge.12596 -
NLM
Lehallea D, Wieczorek D, Zechi-Ceide RM, Passos-Bueno MR, Lyonnet S, Amie J, Gordon CT. A review of craniofacial disorders caused by spliceosomal defects [Internet]. Clinical Genetics. 2015 ; on-line.[citado 2026 fev. 14 ] Available from: https://doi.org/10.1111/cge.12596 -
Vancouver
Lehallea D, Wieczorek D, Zechi-Ceide RM, Passos-Bueno MR, Lyonnet S, Amie J, Gordon CT. A review of craniofacial disorders caused by spliceosomal defects [Internet]. Clinical Genetics. 2015 ; on-line.[citado 2026 fev. 14 ] Available from: https://doi.org/10.1111/cge.12596 - Cellular interference in craniofrontonasal syndrome: males mosaic for mutations in the X-linked EFNB1 gene are more severely affected than true hemizygotes
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Informações sobre o DOI: 10.1111/cge.12596 (Fonte: oaDOI API)
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