Fernanda T. Bellucco
Sao Paulo, SP, Brazil
Last Updated: 09/26/2026
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Found 22 publications
Ring chromosomes uncovered by optical genome mapping: impact of telomeric-associated regions and reference genome selection on structural variant interpretation.
Journal: Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology
Published: April 08, 2026
Replication-Based Mechanism Underlies a Complex dup(18p)/del(18q) Rearrangement Not Derived From Parental Inversion.
Journal: Molecular syndromology
Published: February 18, 2026
Cytogenomic characterization of karyotypes with additional autosomal material.
Journal: Scientific reports
Published: December 26, 2024
Fold-back mechanism originating inv-dup-del rearrangements in chromosomes 13 and 15.
Journal: Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology
Published: December 21, 2022
Mechanisms of structural chromosomal rearrangement formation.
Journal: Molecular cytogenetics
Published: December 21, 2021
Minimal Critical Region and Genes for a Typical Presentation of Langer-Giedion Syndrome.
Journal: Cytogenetic and genome research
Published: September 17, 2021
Correction to: Serologic evidence of West Nile virus and Saint Louis encephalitis virus in horses from Southern Brazil.
Journal: Brazilian journal of microbiology : [publication of the Brazilian Society for Microbiology]
Published: April 28, 2021
Antibody indexes in COVID-19 convalescent plasma donors: Unanswered questions.
Journal: Clinics (Sao Paulo, Brazil)
Published: January 22, 2021
Spread of X-chromosome inactivation into autosomal regions in patients with unbalanced X-autosome translocations and its phenotypic effects.
Journal: American journal of medical genetics. Part A
Published: December 23, 2020
Serologic evidence of West Nile virus and Saint Louis encephalitis virus in horses from Southern Brazil.
Journal: Brazilian journal of microbiology : [publication of the Brazilian Society for Microbiology]
Published: August 12, 2020
Partial 5p Gain and 15q Loss in Three Patients from a Family with a t(5;15)(p13.3;q26.3) Translocation.
Journal: Cytogenetic and genome research
Published: April 08, 2020
Malan syndrome in a patient with 19p13.2p13.12 deletion encompassing NFIX and CACNA1A genes: Case report and review of the literature.
Journal: Molecular genetics & genomic medicine
Published: July 30, 2019
Last Updated: 09/26/2026