Társis Paiva Vieira

Defining new guidelines for screening the 22q11.2 deletion based on a clinical and dysmorphologic evaluation of 194 individuals and review of the literature

Fabíola Paoli Monteiro, Társis Paiva Vieira, Ilária Cristina Sgardioli et al. · European Journal of Pediatrics · 2013 · 68 citations

Public Health, Psychiatry, Genetic Counseling +6

Genomic imbalances in syndromic congenital heart disease

Miriam Coelho Molck, Milena Simioni, Társis Paiva Vieira et al. · Jornal de Pediatria · 2017 · 49 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

OCT4 immunohistochemistry may be necessary to identify the real risk of gonadal tumors in patients with Turner syndrome and Y chromosome sequences

Beatriz Amstalden Barros, Suzana Guimarães Moraes, Fernanda Boechers Coeli et al. · Human Reproduction · 2011 · 31 citations

Medicine, Genetics, Pathology +17

Clinical Features in Patients with 22q11.2 Deletion Syndrome Ascertained by Palatal Abnormalities

Társis Paiva Vieira, Fabíola Paoli Monteiro, Ilária Cristina Sgardioli et al. · The Cleft Palate-Craniofacial Journal · 2014 · 28 citations

Life Sciences, Genetics, Molecular Genetics +15

Insertional translocation of 15q25‐q26 into 11p13 and duplication at 8p23.1 characterized by high resolution arrays in a boy with congenital malformations and aniridia

Milena Simioni, Társis Paiva Vieira, Ilária Cristina Sgardioli et al. · American Journal of Medical Genetics Part A · 2012 · 23 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15