Mayara J. Prado
Bento Gonçalves Avenue 9500
Porto Alegre, RS 91501970, Brazil
Porto Alegre, RS 91501970, Brazil
Last Updated: 09/26/2026
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Found 10 publications
APOL1 G1/G2 Variants Associated With CKD in Afro-Brazilians.
Journal: Kidney international reports
Published: April 17, 2025
Variant predictions in congenital adrenal hyperplasia caused by mutations in CYP21A2.
Journal: Frontiers in pharmacology
Published: May 02, 2022
Characterization of Mutations Causing CYP21A2 Deficiency in Brazilian and Portuguese Populations.
Journal: International journal of molecular sciences
Published: December 07, 2021
Novel frameshift variant of the CFTR gene: S511Lfs*2 from phenotype to molecular predictions.
Journal: Molecular biology reports
Published: March 27, 2020
Cystic Fibrosis: A Simple and Customized Strategy for Genetic Screening Able to Detect Over 90% of Identified Mutated Alleles in Brazilian Newborns.
Journal: Molecular diagnosis & therapy
Published: March 19, 2020
A Low-Cost and Simple Genetic Screening for Cystic Fibrosis Provided by the Brazilian Public Health System.
Journal: The Journal of pediatrics
Published: October 20, 2017
Development of CYP21A2 Genotyping Assay for the Diagnosis of Congenital Adrenal Hyperplasia.
Journal: Molecular diagnosis & therapy
Published: August 19, 2017
Clinical and molecular profile of newborns with confirmed or suspicious congenital adrenal hyperplasia detected after a public screening program implementation.
Journal: Jornal de pediatria
Published: April 30, 2017
Showing 1-10 of 10
Last Updated: 09/26/2026