Roberta Lelis Dutra
Publications by Year
Research Areas
Genomic variations and chromosomal abnormalities, Williams Syndrome Research, Congenital heart defects research, Congenital Heart Disease Studies, Prenatal Screening and Diagnostics
Most-Cited Works
- → FGFR4 Profile as a Prognostic Marker in Squamous Cell Carcinoma of the Mouth and Oropharynx(2012)33 cited
- → Detection of deletions at 7q11.23 in Williams-Beuren syndrome by polymorphic markers(2011)31 cited
- → Copy number variation in Williams-Beuren syndrome: suitable diagnostic strategy for developing countries(2012)27 cited
- → Congenital Heart Disease as a Warning Sign for the Diagnosis of the 22q11.2 Deletion(2014)23 cited
- → Williams-Beuren Syndrome: A Clinical Study of 55 Brazilian Patients and the Diagnostic Use of MLPA(2015)23 cited
- → Investigation of copy number variation in children with conotruncal heart defects(2014)22 cited
- → Complex structural rearrangement features suggesting chromoanagenesis mechanism in a case of 1p36 deletion syndrome(2014)19 cited
- → Cytogenomic assessment of the diagnosis of 93 patients with developmental delay and multiple congenital abnormalities: The Brazilian experience(2017)16 cited
- → Cytogenomic delineation and clinical follow-up of 10 Brazilian patients with Pallister-Killian syndrome(2015)13 cited
- → Atypical Deletion in Williams–Beuren Syndrome Critical Region Detected by MLPA in a Patient with Supravalvular Aortic Stenosis and Learning Difficulty(2012)12 cited