Detalhe da pesquisa
1.
Analysis of cardiac anomalies in VACTERL association.
Birth Defects Res A Clin Mol Teratol
; 97(12): 792-7, 2013 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-24343877
2.
Holoprosencephaly in a family segregating novel variants in ZIC2 and GLI2.
Am J Med Genet A
; 155A(4): 860-4, 2011 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-21416594
3.
An approach to the identification of anomalies and etiologies in neonates with identified or suspected VACTERL (vertebral defects, anal atresia, tracheo-esophageal fistula with esophageal atresia, cardiac anomalies, renal anomalies, and limb anomalies) association.
J Pediatr
; 164(3): 451-7.e1, 2014 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-24332453
4.
Analysis of FOXF1 and the FOX gene cluster in patients with VACTERL association.
Eur J Med Genet
; 54(3): 323-8, 2011.
Artigo
em Inglês
| MEDLINE | ID: mdl-21315191