Detalhe da pesquisa
1.
Population-based prevalence surveys during the Covid-19 pandemic: A systematic review.
Rev Med Virol
; 31(4): e2200, 2021 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-34260777
2.
Candidate genes of oculo-auriculo-vertebral spectrum in 22q region: A systematic review.
Am J Med Genet A
; 182(11): 2624-2631, 2020 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-32893956
3.
Congenital Heart Defects and 22q11.2 Deletion Syndrome: A 20-Year Update and New Insights to Aid Clinical Diagnosis.
J Pediatr Genet
; 12(2): 113-122, 2023 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-37090828
4.
Hospital characteristics associated with COVID-19 mortality: data from the multicenter cohort Brazilian Registry.
Intern Emerg Med
; 17(8): 2299-2313, 2022 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-36153772
5.
Pseudohypoparathyroidism with Ectopic Calcification and 22q11 Deletion Syndrome: A Rare Case.
J Pediatr Genet
; 10(1): 45-48, 2021 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-33552638
6.
A child with cat-eye syndrome and oculo-auriculo-vertebral spectrum phenotype: A discussion around molecular cytogenetic findings.
Eur J Med Genet
; 64(11): 104319, 2021 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-34474176
7.
Microarray-Based Comparative Genomic Hybridization, Multiplex Ligation-Dependent Probe Amplification, and High-Resolution Karyotype for Differential Diagnosis Oculoauriculovertebral Spectrum: A Systematic Review.
J Pediatr Genet
; 9(3): 149-157, 2020 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-32714614
8.
Congenital Heart Defects and Dysmorphic Facial Features in Patients Suspicious of 22q11.2 Deletion Syndrome in Southern Brazil.
J Pediatr Genet
; 9(4): 227-234, 2020 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-32733742