Rubinstein-Taybi syndrome with deletions of FISH probe RT1 at 16p13.3: two UK patients.
Open Access
- 1 January 1996
- journal article
- research article
- Published by BMJ in Journal of Medical Genetics
- Vol. 33 (1) , 82-83
- https://doi.org/10.1136/jmg.33.1.82
Abstract
We report two patients with Rubinstein-Taybi syndrome out of a total of 16 tested who have a deletion of the region visualised by the cosmid probe RT1. These results further confirm this as a locus for Rubinstein-Taybi syndrome.Keywords
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