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Delineation of a 50 kilobase DNA segment containing the recombination site in a sporadic case of Huntington's disease

Weber, Bernhard H. F. , Riess, O, Wolff, G, Andrew, S, Collins, C, Graham, R, Theilman, J and Hayden, M R (1992) Delineation of a 50 kilobase DNA segment containing the recombination site in a sporadic case of Huntington's disease. Nature Genetics 2, pp. 216-222.

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Abstract

No detectable rearrangements involving chromosome 4p16.3 have been observed in patients with Huntington's disease (HD). New mutations for HD could involve structural alterations which might aid the localization of the defective gene. We have reinvestigated a well documented sporadic case of HD. DNA haplotyping with markers between D4S10 and the telomeric locus D4S141 reveals a recombination event ...

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Item type:Article
Date:1992
Institutions:Medicine > Lehrstuhl für Humangenetik
Identification Number:
ValueType
10.1038/ng1192-216DOI
1345172PubMed ID
Dewey Decimal Classification:600 Technology > 610 Medical sciences Medicine
Status:Published
Refereed:Yes, this version has been refereed
Created at the University of Regensburg:No
Item ID:35365
Owner only: item control page
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