Source: Cytogenetic and Genome Research. Unidade: IB
Assunto: ANORMALIDADES CROMOSSÔMICAS
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KREPISCHI, Ana Cristina Victorino et al. Whole-genome array-CGH screening in undiagnosed syndromic patients: old syndromes revisited and new alterations. Cytogenetic and Genome Research, v. 115, n. 3-4, p. 254-261, 2006Tradução . . Disponível em: https://doi.org/10.1159/000095922. Acesso em: 27 set. 2024.APA
Krepischi, A. C. V., Vianna-Morgante, A. M., Jehee, F. S., Passos-Bueno, M. R., Knijnenburg, J., Szuhai, K., et al. (2006). Whole-genome array-CGH screening in undiagnosed syndromic patients: old syndromes revisited and new alterations. Cytogenetic and Genome Research, 115( 3-4), 254-261. doi:10.1159/000095922NLM
Krepischi ACV, Vianna-Morgante AM, Jehee FS, Passos-Bueno MR, Knijnenburg J, Szuhai K, Sloos W, Mazzeu JF, Kok F, Cheroki C, Otto PA, Mingroni Netto RC, Varela MC, Koiffmann CP, Kim CA, Bertola DR, Pearson PL. Whole-genome array-CGH screening in undiagnosed syndromic patients: old syndromes revisited and new alterations [Internet]. Cytogenetic and Genome Research. 2006 ; 115( 3-4): 254-261.[citado 2024 set. 27 ] Available from: https://doi.org/10.1159/000095922Vancouver
Krepischi ACV, Vianna-Morgante AM, Jehee FS, Passos-Bueno MR, Knijnenburg J, Szuhai K, Sloos W, Mazzeu JF, Kok F, Cheroki C, Otto PA, Mingroni Netto RC, Varela MC, Koiffmann CP, Kim CA, Bertola DR, Pearson PL. Whole-genome array-CGH screening in undiagnosed syndromic patients: old syndromes revisited and new alterations [Internet]. Cytogenetic and Genome Research. 2006 ; 115( 3-4): 254-261.[citado 2024 set. 27 ] Available from: https://doi.org/10.1159/000095922