Twigg, Stephen R. F.; Babbs, Christian; Elzen, Marijke E. P. van den; Goriely, Anne; Taylor, Stephen; McGowan, Simon J.; Giannoulatou, Eleni; Lonie, Lorne; Ragoussis, Jiannis; Akha, Elham Sadighi; Knight, Samantha J. L.; Zechi-Ceide, Roseli Maria 
; Hoogeboom, Jeannette A. M.; Pober, Barbara R.; Toriello, Helga V.; Wall, Steven A.; Passos-Bueno, Maria Rita ; Brunner, Han G.; Mathijssen, Irene M. J.; Wilkie, Andrew O. M.
Source: Human Molecular Genetics. Unidades: HRAC, IB
Subjects: GENÉTICA, ANORMALIDADES MÚLTIPLAS, MUTAÇÃO
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TWIGG, Stephen R. F. et al. Cellular interference in craniofrontonasal syndrome: males mosaic for mutations in the X-linked EFNB1 gene are more severely affected than true hemizygotes. Human Molecular Genetics, v. 22, n. 8, p. 1654-1662, 2013Tradução . . Disponível em: https://doi.org/10.1093/hmg/ddt015. Acesso em: 10 jun. 2024.APA
Twigg, S. R. F., Babbs, C., Elzen, M. E. P. van den, Goriely, A., Taylor, S., McGowan, S. J., et al. (2013). Cellular interference in craniofrontonasal syndrome: males mosaic for mutations in the X-linked EFNB1 gene are more severely affected than true hemizygotes. Human Molecular Genetics, 22( 8), 1654-1662. doi:10.1093/hmg/ddt015NLM
Twigg SRF, Babbs C, Elzen MEP van den, Goriely A, Taylor S, McGowan SJ, Giannoulatou E, Lonie L, Ragoussis J, Akha ES, Knight SJL, Zechi-Ceide RM, Hoogeboom JAM, Pober BR, Toriello HV, Wall SA, Passos-Bueno MR, Brunner HG, Mathijssen IMJ, Wilkie AOM. Cellular interference in craniofrontonasal syndrome: males mosaic for mutations in the X-linked EFNB1 gene are more severely affected than true hemizygotes [Internet]. Human Molecular Genetics. 2013 ; 22( 8): 1654-1662.[citado 2024 jun. 10 ] Available from: https://doi.org/10.1093/hmg/ddt015Vancouver
Twigg SRF, Babbs C, Elzen MEP van den, Goriely A, Taylor S, McGowan SJ, Giannoulatou E, Lonie L, Ragoussis J, Akha ES, Knight SJL, Zechi-Ceide RM, Hoogeboom JAM, Pober BR, Toriello HV, Wall SA, Passos-Bueno MR, Brunner HG, Mathijssen IMJ, Wilkie AOM. Cellular interference in craniofrontonasal syndrome: males mosaic for mutations in the X-linked EFNB1 gene are more severely affected than true hemizygotes [Internet]. Human Molecular Genetics. 2013 ; 22( 8): 1654-1662.[citado 2024 jun. 10 ] Available from: https://doi.org/10.1093/hmg/ddt015
