Germline copy number variations and cancer predisposition (2012)
- Authors:
- USP affiliated authors: PEARSON, PETER LEES - IB ; ROSENBERG, CARLA - IB
- Unidade: IB
- DOI: 10.2217/fon.12.34
- Subjects: NEOPLASIAS; GENES; DOENÇAS GENÉTICAS
- Language: Inglês
- Imprenta:
- Source:
- Título: Future Oncology
- ISSN: 1744-8301
- Volume/Número/Paginação/Ano: v. 8, n. 4, p. 441-450, Apr. 2012
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
KREPISCHI, Ana Cristina Victorino e PEARSON, Peter Lees e ROSENBERG, Carla. Germline copy number variations and cancer predisposition. Future Oncology, v. 8, n. 4, p. 441-450, 2012Tradução . . Disponível em: https://doi.org/10.2217/fon.12.34. Acesso em: 28 dez. 2025. -
APA
Krepischi, A. C. V., Pearson, P. L., & Rosenberg, C. (2012). Germline copy number variations and cancer predisposition. Future Oncology, 8( 4), 441-450. doi:10.2217/fon.12.34 -
NLM
Krepischi ACV, Pearson PL, Rosenberg C. Germline copy number variations and cancer predisposition [Internet]. Future Oncology. 2012 ; 8( 4): 441-450.[citado 2025 dez. 28 ] Available from: https://doi.org/10.2217/fon.12.34 -
Vancouver
Krepischi ACV, Pearson PL, Rosenberg C. Germline copy number variations and cancer predisposition [Internet]. Future Oncology. 2012 ; 8( 4): 441-450.[citado 2025 dez. 28 ] Available from: https://doi.org/10.2217/fon.12.34 - Array-CGH analysis in patients with Goldenhar Syndrome
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- Number of rare germline CNVs and TP53 mutation types
- Li-Fraumeni-like syndrome associated with a large BRCA1 intragenic deletion
- Complex phenotype associated with 17q21.31 microdeletion
- High frequency of submicroscopic chromosomal deletions and duplications in dysmorphic patients born small for gestational age
- Desvendado mecanismo de mutação genética ligada à deficiência intelectual. [Depoimento]
- Consensus Statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies
- Subtelomeric 6p25 deletion/duplication: report of a patient with new clinical findings and genotype–phenotype correlations
Informações sobre o DOI: 10.2217/fon.12.34 (Fonte: oaDOI API)
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