Deletions within chromosome 22q11 in familial congenital heart disease
- 5 September 1992
- journal article
- Published by Elsevier in The Lancet
- Vol. 340 (8819), 573-575
- https://doi.org/10.1016/0140-6736(92)92107-q
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- Velo-cardio-facial syndrome associated with chromosome 22 deletions encompassing the DiGeorge locusThe Lancet, 1992
- DiGeorge syndrome with isolated aortic coarctation and isolated ventricular septal defect in three sibs with a 22q11 deletion of maternal origin.Heart, 1991
- Velocardiofacial (Shprintzen) syndrome: an important syndrome for the dysmorphologist to recognise.Journal of Medical Genetics, 1991
- Hereditary unstable DNA: a new explanation for some old genetic questions?The Lancet, 1991
- Prevalence of significant congenital heart defects in children of parents with Fallot's tetralogyThe American Journal of Cardiology, 1990
- Pregnancy and its outcome in women with and without surgical treatment of congenital heart diseaseThe American Journal of Cardiology, 1982
- Study of children of parents operated on for congenital cardiovascular malformations.Heart, 1982
- Risks to the offspring of patients with some common congenital heart defects.Journal of Medical Genetics, 1981
- The spectrum of the DiGeorge syndromeThe Journal of Pediatrics, 1979