Insight into the mechanisms and consequences of recurrent telomere capture associated with a sub-telomeric deletion (2018)
- Authors:
- USP affiliated authors: KREPISCHI, ANA CRISTINA VICTORINO - IB ; MORGANTE, ANGELA MARIA VIANNA - IB ; OTTO, PAULO ALBERTO - IB ; ROSENBERG, CARLA - IB
- Unidade: IB
- DOI: 10.1007/s10577-018-9578-z
- Subjects: TELÔMERO; ANORMALIDADES CROMOSSÔMICAS; DOENÇAS GENÉTICAS
- Keywords: Telomere capture; UPD; Mosaicism; SNP microarray
- Agências de fomento:
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Chromosome Research
- ISSN: 0967-3849
- Volume/Número/Paginação/Ano: v. 26, p. 191-198, 2018
- Este periódico é de assinatura
- Este artigo é de acesso aberto
- URL de acesso aberto
- Cor do Acesso Aberto: green
- Licença: other-oa
-
ABNT
SANTOS, Alexsandro dos et al. Insight into the mechanisms and consequences of recurrent telomere capture associated with a sub-telomeric deletion. Chromosome Research, v. 26, p. 191-198, 2018Tradução . . Disponível em: https://doi.org/10.1007/s10577-018-9578-z. Acesso em: 18 abr. 2024. -
APA
Santos, A. dos, Campagnari, F., Krepischi, A. C. V., Câmara, M. de L. R., Brasil, R. de C. E. de A., Vieira, L., et al. (2018). Insight into the mechanisms and consequences of recurrent telomere capture associated with a sub-telomeric deletion. Chromosome Research, 26, 191-198. doi:10.1007/s10577-018-9578-z -
NLM
Santos A dos, Campagnari F, Krepischi ACV, Câmara M de LR, Brasil R de CE de A, Vieira L, Vianna-Morgante AM, Otto PA, Pearson PL, Rosenberg C. Insight into the mechanisms and consequences of recurrent telomere capture associated with a sub-telomeric deletion [Internet]. Chromosome Research. 2018 ; 26 191-198.[citado 2024 abr. 18 ] Available from: https://doi.org/10.1007/s10577-018-9578-z -
Vancouver
Santos A dos, Campagnari F, Krepischi ACV, Câmara M de LR, Brasil R de CE de A, Vieira L, Vianna-Morgante AM, Otto PA, Pearson PL, Rosenberg C. Insight into the mechanisms and consequences of recurrent telomere capture associated with a sub-telomeric deletion [Internet]. Chromosome Research. 2018 ; 26 191-198.[citado 2024 abr. 18 ] Available from: https://doi.org/10.1007/s10577-018-9578-z - Homozygous duplication at 10p11.21 in a boy clinical manifestations of Lin-Gettig syndrome
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Informações sobre o DOI: 10.1007/s10577-018-9578-z (Fonte: oaDOI API)
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