Freitas, E.L.; Uehara, D.T.; Dantas, V.G.L.; Silva, A.G.; Krepischi, Ana Cristina Victorino 
; Mingroni Netto, Regina Celia ; Rosenberg, Carla
Source: Posters: Cytogenetics. Conference titles: Annual Meeting of the American Society of Human Genetics. Unidade: IB
Subjects: PERDA AUDITIVA, GENÉTICA MÉDICA, CITOGENÉTICA
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ABNT
FREITAS, E.L. et al. Whole-genome array-CGH screening in patients with autosomal dominant sensorineural hearing loss points to novel susceptibility loci. 2012, Anais.. São Francisco: Instituto de Biociências, Universidade de São Paulo, 2012. Disponível em: http://www.ashg.org/2012meeting/pdf/38731_poster_complete.pdf. Acesso em: 06 nov. 2024.APA
Freitas, E. L., Uehara, D. T., Dantas, V. G. L., Silva, A. G., Krepischi, A. C. V., Mingroni Netto, R. C., & Rosenberg, C. (2012). Whole-genome array-CGH screening in patients with autosomal dominant sensorineural hearing loss points to novel susceptibility loci. In Posters: Cytogenetics. São Francisco: Instituto de Biociências, Universidade de São Paulo. Recuperado de http://www.ashg.org/2012meeting/pdf/38731_poster_complete.pdfNLM
Freitas EL, Uehara DT, Dantas VGL, Silva AG, Krepischi ACV, Mingroni Netto RC, Rosenberg C. Whole-genome array-CGH screening in patients with autosomal dominant sensorineural hearing loss points to novel susceptibility loci [Internet]. Posters: Cytogenetics. 2012 ;[citado 2024 nov. 06 ] Available from: http://www.ashg.org/2012meeting/pdf/38731_poster_complete.pdfVancouver
Freitas EL, Uehara DT, Dantas VGL, Silva AG, Krepischi ACV, Mingroni Netto RC, Rosenberg C. Whole-genome array-CGH screening in patients with autosomal dominant sensorineural hearing loss points to novel susceptibility loci [Internet]. Posters: Cytogenetics. 2012 ;[citado 2024 nov. 06 ] Available from: http://www.ashg.org/2012meeting/pdf/38731_poster_complete.pdf
