Cosegregation of hypertrophic cardiomyopathy and a fragile site on chromosome 16 in a large Italian family.
- 1 June 1990
- journal article
- research article
- Published by BMJ in Journal of Medical Genetics
- Vol. 27 (6) , 363-366
- https://doi.org/10.1136/jmg.27.6.363
Abstract
We studied the karyotypes of 10 members of a family in whom hypertrophic cardiomyopathy is segregating as an autosomal dominant trait. In all those affected by the disease, a fragile site on the long arm of chromosome 16 was found, expressed with different frequencies, but the unaffected family members did not show this trait.This publication has 16 references indexed in Scilit:
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