Genetic testing for idiopathic intellectual disability: use of DNA extracted from saliva for SNP Genotyping (2014)
- Authors:
- USP affiliated authors: KREPISCHI, ANA CRISTINA VICTORINO - IB ; ROSENBERG, CARLA - IB
- Unidade: IB
- Subjects: DNA; GENÉTICA
- Language: Português
- Imprenta:
- Source:
- Título do periódico: Resumo
- Conference titles: Congresso Brasileiro de Genética
-
ABNT
SANTOS, A. et al. Genetic testing for idiopathic intellectual disability: use of DNA extracted from saliva for SNP Genotyping. 2014, Anais.. Guarujá: Instituto de Biociências, Universidade de São Paulo, 2014. . Acesso em: 24 jul. 2024. -
APA
Santos, A., Campagnari, F., Câmara, M. L. R. C., Brasil, R. C. E. Z., Krepischi, A. C. V., & Rosenberg, C. (2014). Genetic testing for idiopathic intellectual disability: use of DNA extracted from saliva for SNP Genotyping. In Resumo. Guarujá: Instituto de Biociências, Universidade de São Paulo. -
NLM
Santos A, Campagnari F, Câmara MLRC, Brasil RCEZ, Krepischi ACV, Rosenberg C. Genetic testing for idiopathic intellectual disability: use of DNA extracted from saliva for SNP Genotyping. Resumo. 2014 ;[citado 2024 jul. 24 ] -
Vancouver
Santos A, Campagnari F, Câmara MLRC, Brasil RCEZ, Krepischi ACV, Rosenberg C. Genetic testing for idiopathic intellectual disability: use of DNA extracted from saliva for SNP Genotyping. Resumo. 2014 ;[citado 2024 jul. 24 ] - Cytogenetically visible inversions are formed by multiple molecular mechanisms
- LINE-1 hypermethylation in peripheral blood of cutaneous melanoma patients is associated with metastasis
- Rare germline copy number variations in hereditary cutaneous melanoma
- Lymphovascular invasion and histologic grade are associated with specific genomic profiles in invasive carcinomas of the breast
- An apparently balanced complex chromosome rearrangement involving seven breaks and four chromosomes in a healthy female and segregation/recombination in her affected son
- Upregulated genes at 2q24 gains as candidate oncogenes in hepatoblastomas
- Low frequency of germline TERT and MITF mutations in Brazilian melanoma-prone patients
- Does increase in genomic microarray resolution result in increased diagnostic yield?
- Insights into the somatic mutation burden of hepatoblastomas using whole exome sequencing
- Genotype–phenotype correlation of 16p13.3 terminal duplication and 22q13.33 deletion: natural history of a patient and review of the literature
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas