Silviene F. De Oliveira
Brasilia, DF, Brazil
Last Updated: 09/26/2026
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Found 18 publications
Mayer-Rokitansky-Küster-Hauser syndrome associated with 7q11.23 microduplication: A case report.
Journal: Global medical genetics
Published: December 09, 2024
Advances in forensic genetics: Exploring the potential of long read sequencing.
Journal: Forensic science international. Genetics
Published: May 03, 2024
Retraction Note: Study of liver toxicity and DNA damage due to exposure to the pesticide Mancozeb in an experimental animal model - A pilot model.
Journal: European review for medical and pharmacological sciences
Published: November 17, 2023
Study of liver toxicity and DNA damage due to exposure to the pesticide Mancozeb in an experimental animal model - A pilot model.
Journal: European review for medical and pharmacological sciences
Published: July 17, 2023
Unequal Impact of COL1A1 and COL1A2 Variants on Dentinogenesis Imperfecta.
Journal: Journal of dental research
Published: March 23, 2023
OSR1 disruption contributes to uterine factor infertility via impaired Müllerian duct development and endometrial receptivity.
Journal: The Journal of clinical investigation
Published: May 13, 2022
Cardiovascular risk factors across different levels of urbanization in Brazilian Afro-derived communities (quilombos).
Journal: American journal of human biology : the official journal of the Human Biology Council
Published: April 28, 2022
ZDHHC9 X-linked intellectual disability: Clinical and molecular characterization.
Journal: American journal of medical genetics. Part A
Published: March 15, 2022
Characterization of Associated Nonclassical Phenotypes in Patients with Deletion in the WAGR Region Identified by Chromosomal Microarray: New Insights and Literature Review.
Journal: Molecular syndromology
Published: March 16, 2021
Defining the Critical Region for Intellectual Disability and Brain Malformations in 6q27 Microdeletions.
Journal: Molecular syndromology
Published: May 07, 2019
A Balanced Reciprocal Translocation t(2;9)(p25;q13) Disrupting the LINC00299 Gene in a Patient with Intellectual Disability.
Journal: Molecular syndromology
Published: March 29, 2019
High Frequency of Copy-Neutral Loss of Heterozygosity in Patients with Myelofibrosis.
Journal: Cytogenetic and genome research
Published: December 19, 2017
Last Updated: 09/26/2026