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. 2016 Jan 23;4(2):197–210. doi: 10.1002/mgg3.195

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© 2016 The Authors. Molecular Genetics & Genomic Medicine published by Wiley Periodicals, Inc.

This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

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Haplotype of pedigree 1, chromosome 2q21.2–q31.1. An approximate 34 cM region from rs2872920 (144.22 cM) to rs17664 (178.74 cM) in chromosome 2q21.2–q31.1 cosegregates identically by descent (IBD) with all of the clinically and EEG affected members in the pedigree. It fails to cosegregate with member 74, the only individual whose phenotype is considered “unknown.” The cosegregating haplotype is in light blue. The upper boundary is demarcated by a recombination in member 56 and the lower boundary by a recombination in member 7. While all markers within the area were analyzed by SimWalk and cosegregate, markers between rs6430398 and rs1401750, and between rs889920 and rs1517342, as well as several markers in the represented region have been removed to condense the figure.