Abstract
In Caucasian children with ventricular septal defect and chromosome 22 deletions, the perimembranous type is the more frequent but the subarterial type and positional anomalies of the aortic arch are prevalent in comparison with patients with non-syndrome forms of ventricular septal defect.
| Original language | English |
|---|---|
| Pages (from-to) | 116-117 |
| Number of pages | 2 |
| Journal | European Journal of Pediatrics |
| Volume | 161 |
| Issue number | 2 |
| DOIs | |
| Publication status | Published - 2002 |
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ASJC Scopus subject areas
- Pediatrics, Perinatology, and Child Health
Cite this
Ventricular septal defect and deletion of chromosome 22q11 : Anatomical types and aortic arch anomalies. / Toscano, Alessandra; Anaclerio, Silvia; Digilio, Maria Cristina; Giannotti, Aldo; Fariello, Giuseppe; Dallapiccola, Bruno; Marino, Bruno.
In: European Journal of Pediatrics, Vol. 161, No. 2, 2002, p. 116-117.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Ventricular septal defect and deletion of chromosome 22q11
T2 - Anatomical types and aortic arch anomalies
AU - Toscano, Alessandra
AU - Anaclerio, Silvia
AU - Digilio, Maria Cristina
AU - Giannotti, Aldo
AU - Fariello, Giuseppe
AU - Dallapiccola, Bruno
AU - Marino, Bruno
PY - 2002
Y1 - 2002
N2 - In Caucasian children with ventricular septal defect and chromosome 22 deletions, the perimembranous type is the more frequent but the subarterial type and positional anomalies of the aortic arch are prevalent in comparison with patients with non-syndrome forms of ventricular septal defect.
AB - In Caucasian children with ventricular septal defect and chromosome 22 deletions, the perimembranous type is the more frequent but the subarterial type and positional anomalies of the aortic arch are prevalent in comparison with patients with non-syndrome forms of ventricular septal defect.
UR - http://www.scopus.com/inward/record.url?scp=0036167391&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0036167391&partnerID=8YFLogxK
U2 - 10.1007/s00431-001-0877-5
DO - 10.1007/s00431-001-0877-5
M3 - Article
C2 - 11954747
AN - SCOPUS:0036167391
VL - 161
SP - 116
EP - 117
JO - European Journal of Pediatrics
JF - European Journal of Pediatrics
SN - 0340-6199
IS - 2
ER -