Gil Monteiro Novo‐Filho

Diagnostic power and clinical impact of exome sequencing in a cohort of 500 patients with rare diseases

Caio Robledo D’Angioli Costa Quaio, Caroline Mônaco Moreira, Gil Monteiro Novo‐Filho et al. · American Journal of Medical Genetics Part C Seminars in Medical Genetics · 2020 · 37 citations

Complex structural rearrangement features suggesting chromoanagenesis mechanism in a case of 1p36 deletion syndrome

Évelin Aline Zanardo, Flávia Piazzon, Roberta Lelis Dutra et al. · Molecular Genetics and Genomics · 2014 · 19 citations

Developmental Anomaly, Chromatin, Chromosome Dynamics +12

Application of Whole-Exome Sequencing in Detecting Copy Number Variants in Patients with Developmental Delay and/or Multiple Congenital Malformations

Évelin Aline Zanardo, Fabíola Paoli Monteiro, Samar Nasser Chehimi et al. · Journal of Molecular Diagnostics · 2020 · 19 citations

Developmental Anomaly, Developmental Biology, Mendelian Disorder +12

Mosaic Trisomy 12 Associated with Overgrowth Detected in Fibroblast Cell Lines

Yanca Gasparini Oliveira, Marília M. Montenegro, Gil Monteiro Novo‐Filho et al. · Cytogenetic and Genome Research · 2019 · 18 citations

Cytogenetics, Pathology, Dermatology +24

Cytogenomic assessment of the diagnosis of 93 patients with developmental delay and multiple congenital abnormalities: The Brazilian experience

Évelin Aline Zanardo, Roberta Lelis Dutra, Flávia Piazzon et al. · Clinics · 2017 · 16 citations · Full text