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1 lements as being important in the genesis of atrioventricular septal defect.
2 have right ventricular (RV) dominance or an atrioventricular septal defect.
3 and that Id2 deficiency in mice could cause atrioventricular septal defects.
4 d DMP is associated with the pathogenesis of atrioventricular septal defects.
5 both Hoxb1 and its paralog Hoxa1 results in atrioventricular septal defects.
6 16, an animal model with a high incidence of atrioventricular septal defects.
7 ce rates were particularly high for isolated atrioventricular septal defects (4 of 5 [80%]) and later
8 e cumulative incidence was 1.1% for complete atrioventricular septal defect, 5.3% for pulmonary atres
9 a group of individuals with DS and complete atrioventricular septal defect and sequenced 2 candidate
10 and 1 each with an interrupted aortic arch, atrioventricular septal defect and severe left ventricul
11 r susceptibility to atrial septal defect and atrioventricular septal defects and C57Bl/6 to muscular
12 ariable in patients with CHD7 mutations, but atrioventricular septal defects and conotruncal heart de
13 genitor specification resulted in atrial and atrioventricular septal defects and hypoplasia of the de
14 ac-specific transcription factor gene, cause atrioventricular septal defects and valve abnormalities
15 y single ventricle heart disease (unbalanced atrioventricular septal defect) and systemic outflow obs
17 ome in borderline left ventricle, unbalanced atrioventricular septal defect, and pulmonary atresia wi
18 th a pleitropic syndrome of progressive RCM, atrioventricular septal defects, and a high prevalence o
19 eat arteries, double-outlet right ventricle, atrioventricular septal defects, and caval vein abnormal
20 icular septal defects, 1.55 (1.21, 1.99) for atrioventricular septal defects, and not statistically s
22 ions identified in a cohort of patients with atrioventricular septal defects as a part of Ellis van C
23 ear-old patient following surgical repair of atrioventricular septal defect at the age of 6 years.
24 and management of right dominant unbalanced atrioventricular septal defect (AVSD) remains challengin
37 Ds revealed by histological analysis include atrioventricular septal defects, DORV, single ventricle
38 ng with diverse cardiac anomalies, including atrioventricular septal defects, Ebstein malformation of
39 for coarctation, ventricular septal defect, atrioventricular septal defect, Fallot, and truncus arte
41 es for CHD: CRELD1, which is associated with atrioventricular septal defect in people with or without
42 e mapped the locus responsible for heritable atrioventricular septal defects in six lines (avc1-6).
43 enchymal protrusion, and partially penetrant atrioventricular septal defects, including ostium primum
45 osition complexes (n=6), previously repaired atrioventricular septal defect (n=3), functionally singl
47 duals and their affected offspring shared an atrioventricular septal defect or a common atrium along
48 bance of situs or segmental connection, with atrioventricular septal defect or with tetralogy of Fall
49 Specifically, genes relevant for atrial and atrioventricular septal defects, patent ductus arteriosu
50 e following defects: atrial, ventricular and atrioventricular septal defects; patent ductus arteriosu
51 tal defects (ratio of RRs, 2.51) but not for atrioventricular septal defects (ratio of RRs, 1.06).
52 tralogy of Fallot repair (n = 250), complete atrioventricular septal defect repair (n = 249), arteria
53 ata4 and Smad4 genetically interact in vivo: atrioventricular septal defects result from endothelial-
55 thalamic hamartoma and microcephaly), heart (atrioventricular septal defect), skeleton (postaxial pol
56 areas, such as patent ductus arteriosus and atrioventricular septal defect, the findings are more pr
57 ease covers studies on subjects ranging from atrioventricular septal defects to zebrafish models.
58 interrupted aortic arch, aortic coarctation, atrioventricular septal defect, truncus arteriosus, aort
60 mmon CHD observed, whereas outflow tract and atrioventricular septal defects were the most prevalent
61 in tetralogy of Fallot, 3.6%; 3) painting in atrioventricular septal defect with Down syndrome, 5.1 %