Detalhe da pesquisa
1.
Heterogeneity of genetic modifiers ensures normal cardiac development.
Circulation
; 121(11): 1313-21, 2010 Mar 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-20212279
2.
Loss of glypican-3 function causes growth factor-dependent defects in cardiac and coronary vascular development.
Dev Biol
; 335(1): 208-15, 2009 Nov 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-19733558
3.
Insights into the treatment of inflammatory bowel disease in pregnancy.
Therap Adv Gastroenterol
; 12: 1756284819852231, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-31191713
4.
Complex trait analysis of ventricular septal defects caused by Nkx2-5 mutation.
Circ Cardiovasc Genet
; 5(3): 293-300, 2012 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-22534315
5.
Molecular genetics of congenital diaphragmatic defects.
Ann Med
; 39(4): 261-74, 2007.
Artigo
em Inglês
| MEDLINE | ID: mdl-17558598
6.
Impaired mesenchymal cell function in Gata4 mutant mice leads to diaphragmatic hernias and primary lung defects.
Dev Biol
; 301(2): 602-14, 2007 Jan 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-17069789
7.
Mice lacking sister chromatid cohesion protein PDS5B exhibit developmental abnormalities reminiscent of Cornelia de Lange syndrome.
Development
; 134(17): 3191-201, 2007 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-17652350