Miriam Coelho Molck

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

Ancestry Informative Marker Panel to Estimate Population Stratification Using Genome‐wide Human Array

Fernanda Bueno Barbosa, Natalia F. Cagnin, Milena Simioni et al. · Annals of Human Genetics · 2017 · 21 citations

Life Sciences, Genetics, Molecular Genetics +14

Atypical copy number abnormalities in 22q11.2 region: Report of three cases

Miriam Coelho Molck, Társis Paiva Vieira, Ilária Cristina Sgardioli et al. · European Journal of Medical Genetics · 2013 · 20 citations

Life Sciences, Genetics, Molecular Genetics +17

8p23.1 Interstitial Deletion in a Patient with Congenital Cardiopathy, Neurobehavioral Disorders, and Minor Signs Suggesting 22q11.2 Deletion Syndrome

Miriam Coelho Molck, Fabíola Paoli Monteiro, Milena Simioni et al. · Journal of Developmental & Behavioral Pediatrics · 2015 · 13 citations

Life Sciences, Genetics, Molecular Genetics +17