Skip to main content
U.S. Department of Energy
Office of Scientific and Technical Information

Long range restriction mapping of 13q14. 2 focused on the Wilson disease region

Journal Article · · Genomics; (United States)
 [1];  [2]
  1. Research Institute, Toronto, Onatrio (Canada)
  2. Research Institute, Toronto, Ontario (Canada) Univ. of Toronto, Ontario (Canada)

The Wilson disease locus (WND) has been mapped by multipoint linkage analysis to a region within 13q14.3 that is flanked proximally by marker D12S21 and distally by marker D13S59 at distances of 0.4 and 1.2 cM, respectively. Long range restriction maps were constructed around these two markers to provide a framework for the detailed physical analysis that will be necessary for the cloning of the gene. The maps, together spanning over 4 Mb, include five newly isolated markers (D13S110, D13S113, D13S194, D13F71S1, and D13S196) and two established markers (D13S56and D13S25) that were previously localized to 13q14.2-q14.3 using a hybrid panel. Markers D13F71S1 and D13S196 map to the region between D13S31 and D13S59 and will therefore be useful for the isolation of YAC, for further molecular studies on Wilson disease. 19 refs., 5 figs., 2 tabs.

OSTI ID:
6974823
Journal Information:
Genomics; (United States), Journal Name: Genomics; (United States) Vol. 16:3; ISSN GNMCEP; ISSN 0888-7543
Country of Publication:
United States
Language:
English

Similar Records

A 4. 5-megabase yeast artificial chromosome contig from human chromosome 13q14. 3 ordering 9 polymorphic microsatellites (22 sequence-tagged sites) tightly linked to the Wilson disease locus
Journal Article · Sun Nov 14 23:00:00 EST 1993 · Proceedings of the National Academy of Sciences of the United States of America; (United States) · OSTI ID:7105271

Polymorphic microsatellites and Wilson disease (WD)
Journal Article · Fri Oct 01 00:00:00 EDT 1993 · American Journal of Human Genetics; (United States) · OSTI ID:5104975

Haplotype studies in Wilson disease
Journal Article · Fri Dec 31 23:00:00 EST 1993 · American Journal of Human Genetics; (United States) · OSTI ID:5052743