Detalhe da pesquisa
1.
Resequencing of VEGFR3 pathway genes implicate GJC2 and FLT4 in the formation of primary congenital chylothorax.
Am J Med Genet A
; 188(5): 1607-1611, 2022 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-34994518
2.
PKD1L1 Is Involved in Congenital Chylothorax.
Cells
; 13(2)2024 01 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-38247840
3.
Exome Survey and Candidate Gene Re-Sequencing Identifies Novel Exstrophy Candidate Genes and Implicates LZTR1 in Disease Formation.
Biomolecules
; 13(7)2023 07 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-37509153
4.
Genome-wide identification of disease-causing copy number variations in 450 individuals with anorectal malformations.
Eur J Hum Genet
; 31(1): 105-111, 2023 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36319675
5.
Re-sequencing of candidate genes FOXF1, HSPA6, HAAO, and KYNU in 522 individuals with VATER/VACTERL, VACTER/VACTERL-like association, and isolated anorectal malformation.
Birth Defects Res
; 114(10): 478-486, 2022 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35362267
6.
Genome-wide association study in patients with posterior urethral valves.
Front Pediatr
; 10: 988374, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36238604
7.
Human exome and mouse embryonic expression data implicate ZFHX3, TRPS1, and CHD7 in human esophageal atresia.
PLoS One
; 15(6): e0234246, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32502225