Molecular analysis of chromosome 11 rearrangements in human aniridia
The cause of the disease in two familial and two sporadic cases of aniridia associated with chromosome 11 rearrangements has been analysed. Since the rearrangements apparently leave the PAX6 gene intact, a cosmid contig encompassing <I>PAX6 </I>was assembled and facilitated mapping of th...
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University of Edinburgh
1996
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| Online Access: | http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.649096 |