Source: Clinical Genetics. Unidade: IB
Subjects: CRANIOSSINOSTOSE, ANOMALIA CRANIOFACIAL
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JEHEE, Fernanda Sarquis et al. Molecular screening for microdeletions at 9p22-p24 and 11q23-q24 in a large cohort of patients with trigonocephaly. Clinical Genetics, v. 67, n. 6, p. 503-510, 2005Tradução . . Disponível em: https://doi.org/10.1111/j.1399-0004.2005.00438.x. Acesso em: 02 nov. 2024.APA
Jehee, F. S., Johnson, D., Cavalcanti, D. P., Sá Moreira, E. de, Alberto, F. L., Kok, F., et al. (2005). Molecular screening for microdeletions at 9p22-p24 and 11q23-q24 in a large cohort of patients with trigonocephaly. Clinical Genetics, 67( 6), 503-510. doi:10.1111/j.1399-0004.2005.00438.xNLM
Jehee FS, Johnson D, Cavalcanti DP, Sá Moreira E de, Alberto FL, Kok F, Kim C, Wall SA, Jabs EW, Boyadjiev SA, Passos-Bueno MR. Molecular screening for microdeletions at 9p22-p24 and 11q23-q24 in a large cohort of patients with trigonocephaly [Internet]. Clinical Genetics. 2005 ; 67( 6): 503-510.[citado 2024 nov. 02 ] Available from: https://doi.org/10.1111/j.1399-0004.2005.00438.xVancouver
Jehee FS, Johnson D, Cavalcanti DP, Sá Moreira E de, Alberto FL, Kok F, Kim C, Wall SA, Jabs EW, Boyadjiev SA, Passos-Bueno MR. Molecular screening for microdeletions at 9p22-p24 and 11q23-q24 in a large cohort of patients with trigonocephaly [Internet]. Clinical Genetics. 2005 ; 67( 6): 503-510.[citado 2024 nov. 02 ] Available from: https://doi.org/10.1111/j.1399-0004.2005.00438.x