Whole-genome array-CGH screening in patients with autosomal dominant sensorineural hearing loss points to novel susceptibility loci (2012)
- Authors:
- USP affiliated authors: NETTO, REGINA CELIA MINGRONI - IB ; ROSENBERG, CARLA - IB
- Unidade: IB
- Subjects: PERDA AUDITIVA; GENÉTICA MÉDICA; CITOGENÉTICA
- Language: Inglês
- Imprenta:
- Publisher place: São Francisco
- Date published: 2012
- Source:
- Título do periódico: Posters: Cytogenetics
- Conference titles: Annual Meeting of the American Society of Human Genetics
-
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: 26 abr. 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.pdf -
NLM
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 abr. 26 ] Available from: http://www.ashg.org/2012meeting/pdf/38731_poster_complete.pdf -
Vancouver
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 abr. 26 ] Available from: http://www.ashg.org/2012meeting/pdf/38731_poster_complete.pdf - Deletion of the entire POU4F3 gene in a familial case of autosomal dominant non-syndromic hearing loss
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