del(18p) syndrome with complex tetralogy of fallot in an infant with 45,X,t(Y;18)(q12;q11.2)
- 1 March 1992
- journal article
- case report
- Published by Wiley in American Journal of Medical Genetics
- Vol. 42 (5) , 665-666
- https://doi.org/10.1002/ajmg.1320420507
Abstract
We report on an infant with multiple congenital anomalies, tetralogy of Fallot, and Karyotype 45,X,t(Y;18)(q12;11.2). The infant's anomalies are consistent with a del(18p) syndrome, except for the exceptional severity of the heart defect.Keywords
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