Detalhe da pesquisa
1.
Analysis of Copy Number Variations by Low-Depth Whole-Genome Sequencing in Fetuses with Congenital Cardiovascular Malformations.
Cytogenet Genome Res
; 160(11-12): 643-649, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-33647914
2.
Copy number variations in the GATA4, NKX2-5, TBX5, BMP4 CRELD1, and 22q11.2 gene regions in Chinese children with sporadic congenital heart disease.
J Clin Lab Anal
; 33(2): e22660, 2019 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-30221396