An apparently nonsyndromic infant with the association of anorectal and cardiovascular anomalies and a 22q11 deletion
Am J Med Genet
.
2002 Sep 15;112(1):114-5.
doi: 10.1002/ajmg.10620.
Authors
Luca Rosti
,
Roberta M Bini
,
Alessandro Giamberti
,
Alessandro Frigiola
,
Mario Carminati
PMID:
12239734
DOI:
10.1002/ajmg.10620
No abstract available
Publication types
Case Reports
Letter
MeSH terms
Anal Canal / abnormalities*
Chromosome Deletion*
Chromosomes, Human, Pair 22*
Female
Heart Defects, Congenital / diagnosis*
Humans
Infant, Newborn
Rectum / abnormalities*