B. L. Diniz

22q11 Copy Number Variations in a Brazilian Cohort of Children with Congenital Heart Disorders

M. Floriani, A. S. Santos, B. L. Diniz, 2022, Molecular Syndromology.

Congenital Heart Defects and Dysmorphic Facial Features in Patients Suspicious of 22q11.2 Deletion Syndrome in Southern Brazil

R. Rosa, P. Zen, J. Josahkian, 2020, Journal of Pediatric Genetics.

Candidate genes of oculo‐auriculo‐vertebral spectrum in 22q region: A systematic review

R. Rosa, P. Zen, A. S. Santos, 2020, American journal of medical genetics. Part A.

Microarray-Based Comparative Genomic Hybridization, Multiplex Ligation-Dependent Probe Amplification, and High-Resolution Karyotype for Differential Diagnosis Oculoauriculovertebral Spectrum: A Systematic Review

R. Rosa, P. Zen, A. S. Santos, 2020, Journal of Pediatric Genetics.

Autopsy findings of a child with left atrial isomerism associated with pulmonary agenesis

R. Rosa, P. Zen, R. C. Rosa, 2018 .

Increased levels of chitotriosidase in a patient with Alagille syndrome: association or coincidence?

R. Rosa, P. Zen, M. Floriani, 2018 .

Fluorescence in situ hybridization (FISH) as an irreplaceable diagnostic tool for Williams-Beuren syndrome in developing countries: a literature review

P. Zen, P. Silva, B. L. Diniz, 2023, Revista paulista de pediatria : orgao oficial da Sociedade de Pediatria de Sao Paulo.

Congenital Heart Defects and 22q11.2 Deletion Syndrome: A 20-Year Update and New Insights to Aid Clinical Diagnosis

R. Rosa, P. Zen, B. L. Diniz, 2021, Journal of Pediatric Genetics.