Genomic copy number alterations in non-syndromic hearing loss (2015)
- Authors:
- USP affiliated authors: ROSENBERG, CARLA - IB ; AURICCHIO, MARIA TERESA BALESTER DE MELLO - IB ; KREPISCHI, ANA CRISTINA VICTORINO - IB ; NETTO, REGINA CELIA MINGRONI - IB
- Unidade: IB
- DOI: 10.1111/cge.12683
- Subjects: PERDA AUDITIVA; SURDEZ; GENES; GENÉTICA MÉDICA
- Language: Inglês
- Imprenta:
- Source:
- Título: Clinical Genetics
- ISSN: 1399-0004
- Volume/Número/Paginação/Ano: v. 89, n. 4, p. 473-477, Apr. 2017
- Este periódico é de acesso aberto
- Este artigo NÃO é de acesso aberto
-
ABNT
ROSENBERG, Carla et al. Genomic copy number alterations in non-syndromic hearing loss. Clinical Genetics, v. 89, n. 4, p. 473-477, 2015Tradução . . Disponível em: https://doi.org/10.1111/cge.12683. Acesso em: 22 jan. 2026. -
APA
Rosenberg, C., Freitas, E. L., Uehara, D. T., Auricchio, M. T. B. M., Costa, S. S., Oiticica, J., et al. (2015). Genomic copy number alterations in non-syndromic hearing loss. Clinical Genetics, 89( 4), 473-477. doi:10.1111/cge.12683 -
NLM
Rosenberg C, Freitas EL, Uehara DT, Auricchio MTBM, Costa SS, Oiticica J, Silva AG, Krepischi ACV, Mingroni Netto RC. Genomic copy number alterations in non-syndromic hearing loss [Internet]. Clinical Genetics. 2015 ; 89( 4): 473-477.[citado 2026 jan. 22 ] Available from: https://doi.org/10.1111/cge.12683 -
Vancouver
Rosenberg C, Freitas EL, Uehara DT, Auricchio MTBM, Costa SS, Oiticica J, Silva AG, Krepischi ACV, Mingroni Netto RC. Genomic copy number alterations in non-syndromic hearing loss [Internet]. Clinical Genetics. 2015 ; 89( 4): 473-477.[citado 2026 jan. 22 ] Available from: https://doi.org/10.1111/cge.12683 - Multilocus family-based association analysis of seven candidate polymorphisms with essential hypertension in an African-derived semi-isolated Brazilian population
- Genomic ancestry of rural african-derived populations from Southeastern Brazil
- Multilocus effects of seven polymorphisms on essential hypertension in rural semi-isolated African-derived Brazilian populations: a family-based analysis
- The importance of genetic studies in children with hearing loss ascertained after universal neonatal hearing screening (UNHS)
- Investigating deafness genes as a cause of sudden sensorineural hearing loss
- Inferring paternal history of rural african-derived brazilian populations from y chromosomes
- Multilocus analyses of seven candidate genes suggest interacting pathways for obesity-related traits in brazilian populations
- Investigating deafness genes as a cause of sudden sensorineural hearing loss
- Aberrant transcript produced by a splice donor site deletion in the TECTA gene is associated with autosomal dominat deafness in a Brazilian family
- Genomic ancestry of rural african-derived populations from southeastern Brazil
Informações sobre o DOI: 10.1111/cge.12683 (Fonte: oaDOI API)
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