Browsing by Author "Vargas, Fernando R."
Now showing items 1-11 of 11
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ATXN3, ATXN7, CACNA1A, and RAI1 Genes and Mitochondrial Polymorphism A10398G Did Not Modify Age at Onset in Spinocerebellar Ataxia Type 2 Patients from South America
Pereira, Fernanda S. et al. | Date Issued: 2015 -
Biomarkers of genome instability and cancer epigenetics
Reis, Adriana H. O. et al. | Date Issued: 2016 -
Constitutional and somatic methylation status of DMRH19 and KvDMR in Wilms tumor patients
Cardoso, Leila C. A. et al. | Date Issued: 2011 -
Corpus callosum dysgenesis causes novel patterns of structural and functional brain connectivity
Szczupak, Diego et al. | Date Issued: 2021 -
Cytogenetic and molecular studies of an X;21 translocation previously diagnosed as complete monosomy 21
Camilo, Maria Jesus E. et al. | Date Issued: 2009 -
Influence of estrogen and variations at the BRCA1 promoter region on transcription and translation
Fernandes, Lívia R. et al. | Date Issued: 2014 -
NESSCA Validation and Responsiveness of Several Rating Scales in Spinocerebellar Ataxia Type 2
Monte, Thais L. et al. | Date Issued: 2017 -
Prevalence of the BRCA1 founder mutation c.5266dupin Brazilian individuals at-risk for the hereditary breast and ovarian cancer syndrome
Ewald, Ingrid P. et al. | Date Issued: 2011 -
RFC-1 80G>A polymorphism in case-mother/control-mother dyads is associated with risk of nephroblastoma and neuroblastoma
Azevedo, Rafaela Montalvão de et al. | Date Issued: 2015 -
Síndrome de Down - análise clínica, citogenéticae epidemiológica de 165 casos
Boy, Raquel et al. | Date Issued: 1995Realizou-se retrospectivamente um acompanhamento clínico de 165 pacientes com Síndrome de Down (SD) em um programa ambulatorial no Centro de Genética Médica (IFF - FIOCRUZ). Foram realizadas investigações clínicas e ... -
TP53 germline and somatic mutations in a patient with fibrolamellar hepatocellular carcinoma
Andrade, Raissa C. et al. | Date Issued: 2018