graduation at Biomedicina from Universidade Federal de São Paulo (2021). (Source: Lattes Curriculum)
| News published in Agência FAPESP Newsletter about the researcher |
| TITULO |
| Articles published in other media outlets (0 total): |
| More itemsLess items |
| VEICULO: TITULO (DATA) |
| VEICULO: TITULO (DATA) |
Coesinopathies is the name given to diseases caused by mutations in genes that are part of the protein complex called cohesin or its regulators. This complex has several functions in cellular activity and maintenance of genomic architecture. Because they are syndromes caused by mutations that affect the same structure, the phenotypes of coesinopathies often overlap, making clinical diagno…
The 22q11.2 deletion syndrome is caused by the loss of DNA segments from a region of chromosome 22 that contains LCRs, or segmental duplications, with deletions of 3 Mb and 1.5 Mb of DNA being more frequent. The phenotypic expression of the syndrome is very heterogeneous, and does not seem to be related to the size of the deletions, being very variable even in patients with similar deleti…
A great challenge for cytogeneticists is to understand the genetic basis of the phenotypic variations and its implication for human diseases. Chromosomal rearrangements are an efficient tool for the investigation of the consequences of deletion, duplication or disruption of genes. This project contains three subprojects as follows: Subproject 1: Analysis of women with balanced X-autosome …
| 1 / 1 | Ongoing scholarships in Brazil |
| 2 / 2 | Completed scholarships in Brazil |
| 3 / 3 | All Scholarships |
| Associated processes | |
CV Lattes
ORCID