Detalhe da pesquisa
1.
Low-pass whole genome sequencing is a reliable and cost-effective approach for copy number variant analysis in the clinical setting.
Ann Hum Genet
; 88(2): 113-125, 2024 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-37807935
2.
Congenital chromoanagenesis in the routine postnatal chromosomal microarray analyses.
Am J Med Genet A
; 185(8): 2335-2344, 2021 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-33988290
3.
Chromosomal microarray analyses from 5778 patients with neurodevelopmental disorders and congenital anomalies in Brazil.
Sci Rep
; 12(1): 15184, 2022 09 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-36071085