publicações selecionadas
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Candidate genes of
oculo-auriculo-vertebral spectrum in 22q region: A systematic review - A child with cat-eye syndrome and oculo-auriculo-vertebral spectrum phenotype: A discussion around molecular cytogenetic findings
- 22q11 Copy Number Variations in a Brazilian Cohort of Children with Congenital Heart Disorders
- Development and validation of homebrew FISH Probes for 22q11.2 deletion syndrome
- Population¿based prevalence surveys during the Covid¿19 pandemic: A systematic review
- Microarray-Based Comparative Genomic Hybridization, Multiplex Ligation-Dependent Probe Amplification, and High-Resolution Karyotype for Differential Diagnosis Oculoauriculovertebral Spectrum: A Systematic Review
- Congenital Heart Defects and Dysmorphic Facial Features in Patients Suspicious of 22q11.2 Deletion Syndrome in Southern Brazil