Marília M. Montenegro

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

Cytogenomic delineation and clinical follow-up of 10 Brazilian patients with Pallister-Killian syndrome

Larissa Sampaio de Athayde Costa, Aline Cristina Zandoná-Teixeira, Marília M. Montenegro et al. · Molecular Cytogenetics · 2015 · 13 citations · Full text