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Human Genomics|June 13, 2024
Next-generation sequencing profiling of miRNAs in individuals with 22q11.2 deletion syndrome revealed altered expression of miR-185-5pAnelisa Gollo Dantas, Beatriz Carvalho Nunes, Natália Nunes, et al.Journal of Applied Genetics|August 29, 2015
Position effect modifying gene expression in a patient with ring chromosome 14Roberta Santos Guilherme, Mariana Moysés-Oliveira, Anelisa Gollo Dantas, et al.European Journal of Medical Genetics|January 30, 2022
CEDNIK syndrome in a Brazilian patient with compound heterozygous pathogenic variantsNatália Nunes, Malú Zamariolli, Anelisa Gollo Dantas, et al.Molecular Syndromology|March 22, 2016
22q11.2 Deletion Syndrome due to a Translocation t(6;22) in a Patient Conceived via in vitro FertilizationAnelisa Gollo Dantas, Adriana Bortolai, Mariana Moysés-Oliveira, et al.Genes|May 25, 2024
Neuropsychological Profile of 25 Brazilian Patients with 22q11.2 Deletion Syndrome: Effects of Clinical and Socioeconomic VariablesLarissa Salustiano Evangelista Pimenta, Claudia Berlim de Mello, Luciana Mello Di Benedetto, et al.BMC Medical Genetics|December 21, 2014
Duplication 9p and their implication to phenotypeRoberta Santos Guilherme, Vera Ayres Meloni, Ana Beatriz Alvarez Perez, et al.Fertility and Sterility|March 10, 2015
Genetic mechanisms leading to primary amenorrhea in balanced X-autosome translocationsMariana Moysés-Oliveira, Roberta Dos Santos Guilherme, Anelisa Gollo Dantas, et al.Human Genetics|January 11, 2019
Downregulation of genes outside the deleted region in individuals with 22q11.2 deletion syndromeAnelisa Gollo Dantas, Marcos Leite Santoro, Natalia Nunes, et al.Genetics Research|April 8, 2024
Variants in Candidate Genes for Phenotype Heterogeneity in Patients with the 22q11.2 Deletion SyndromeNatalia Nunes, Beatriz Carvalho Nunes, Malú Zamariolli, et al.Pageof 1