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- Publisher
- Wiley
- Copyright
- 1994 Blackwell Munksgaard
- ISSN
- 0009-9163
- eISSN
- 1399-0004
- DOI
- 10.1111/j.1399-0004.1994.tb04237.x
- Publisher site
- See Article on Publisher Site
Abstract
Holt-Oram syndrome is an autosomal dominant disorder with congenital heart defects and skeletal malformations of the upper extremities. A patient with a deletion of 14q23-24 and Holt-Oram syndrome has been described. In this report, however, genetic linkage to the 14q23-24 region is excluded in a multigeneration family with five available individuals affected with Holt-Oram syndrome. Familial Holt-Oram syndrome might be different from the syndrome with the 14q23-24 deletion.
Journal
Clinical Genetics – Wiley
Published: Sep 1, 1994
Keywords: chromosome 14; Holt-Oram syndrome; linkage analysis