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Mapping of mutation causing Friedreich's ataxia to human chromosome 9

✍ Scribed by Chamberlain, Susan; Shaw, Jacqui; Rowland, Alison; Wallis, Julie; South, Sally; Nakamura, Yusuke; von Gabain, Alexander; Farrall, Martin; Williamson, Robert


Book ID
109755884
Publisher
Nature Publishing Group
Year
1988
Tongue
English
Weight
486 KB
Volume
334
Category
Article
ISSN
0028-0836

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Regional localization by in situ hybridi
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In order to determine the regional localization of the Friedreich's ataxia (FA) gene on chromosome 9, the DNA probe DR47 (D9S5), which detects a restriction fragment length polymorphism (RFLP) in tight linkage with the disease, was hybridized in situ to metaphase chromosomes. Our results enable the