Marshall Ítalo Barros Fontes

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

A multicentric association study between 39 genes and nonsyndromic cleft lip and palate in a Brazilian population

Tânia Kawasaki de Araujo, Rodrigo Secolin, Têmis Maria Félix et al. · Journal of Cranio-Maxillofacial Surgery · 2015 · 59 citations

Dentistry, Genetics, Molecular Genetics +16

Mucopolysaccharidosis type II: Identification of 30 novel mutations among Latin American patients

Ana Carolina Brusius‐Facchin, Ida Vanessa Döederlein Schwartz, Constantin Zimmer et al. · Molecular Genetics and Metabolism · 2013 · 49 citations · Full text

Life Sciences, Genetics, Molecular Genetics +8

Diagnostic implications of associated defects in patients with typical orofacial clefts

Isabella Lopes Monlleó, Amanda G.R. de Barros, Marshall Ítalo Barros Fontes et al. · Jornal de Pediatria · 2015 · 34 citations · Full text

Dentistry, Genetics, Cleft Palate Surgery +16

17p13.3 Microdeletion: Insights on Genotype-Phenotype Correlation

Marshall Ítalo Barros Fontes, Ana Paula dos Santos, Fábio R. Torres et al. · Molecular Syndromology · 2016 · 25 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17