M. Svidnicki

Molecular analysis of SLC26A4 gene in patients with nonsyndromic hearing loss and EVA: identification of two novel mutations in Brazilian patients.

E. Sartorato, N. Z. D. dos Santos, A. Castilho, 2013, International journal of pediatric otorhinolaryngology.

Targeted next-generation sequencing identified novel mutations associated with hereditary anemias in Brazil

F. Costa, S. Saad, S. Saad, 2020, Annals of Hematology.

Karyotypic variability in Iheringichthys labrosus (Teleostei, Pimelodidae) from the Tibagi River basin (Paraná State, Brazil).

M. R. Vicari, R. Artoni, M. C. Almeida, 2008, Genetics and molecular research : GMR.

Etiologic and diagnostic evaluation: Algorithm for severe to profound sensorineural hearing loss in Brazil

E. Sartorato, A. Castilho, M. Soki, 2013, International journal of audiology.

New germline GATA1 variant in females with anemia and thrombocytopenia.

S. Saad, F. Traina, G. R. Assis-Mendonça, 2021, Blood cells, molecules & diseases.

Screening of genetic alterations related to non-syndromic hearing loss using MassARRAY iPLEX® technology

E. Sartorato, N. Z. D. dos Santos, A. Castilho, 2015, BMC Medical Genetics.

Optimization of simultaneous screening of the main mutations involved in non-syndromic deafness using the TaqMan® OpenArray™ Genotyping Platform

E. Sartorato, A. Castilho, F. Martins, 2013, BMC Medical Genetics.

Association between phenotype, performance with hearing aids, and genotype of childhood hearing loss in children with and without genetic alteration.

Eliara Pinto Vieira Biaggio, M. C. Iório, Marisa Frasson de Azevedo, 2012, Jornal da Sociedade Brasileira de Fonoaudiologia.

Study of candidate genes for dyslexia in Brazilian individuals.

R. Secolin, E. Sartorato, S. Ciasca, 2013, Genetics and molecular research : GMR.

Novel mutations associated with pyruvate kinase deficiency in Brazil

S. Brandalise, F. Costa, S. Saad, 2017, Revista brasileira de hematologia e hemoterapia.