Mapping of Charcot-Marie-Tooth Disease Type 1C to Chromosome 16p Identifies a Novel Locus for Demyelinating Neuropathies Valerie A. Street, Jeff D. Goldy,

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Mapping of Charcot-Marie-Tooth Disease Type 1C to Chromosome 16p Identifies a Novel Locus for Demyelinating Neuropathies Valerie A. Street, Jeff D. Goldy, Alana S. Golden, Bruce L Tempel, Thomas D. Bird, Phillip F. Chance The American Journal of Human Genetics Volume 70, Issue 1, Pages 244-250 (January 2002) DOI: 10.1086/337943 Copyright © 2002 The American Society of Human Genetics Terms and Conditions

Figure 1 Haplotype analysis in pedigrees K1550 (A) and K1551 (B). Affected individuals are denoted by blackened symbols, males are denoted by squares, females are denoted by circles, and deceased persons are indicated by a diagonal line through a symbol. Markers are listed from telomere (top) to centromere (bottom) and are the same in both pedigrees. The CMT1C-linked haplotype is boxed. The American Journal of Human Genetics 2002 70, 244-250DOI: (10.1086/337943) Copyright © 2002 The American Society of Human Genetics Terms and Conditions

Figure 2 CMT1C-containing region of 16p. The CMT1C genetic interval on chromosome 16p13.1-p12.3 is indicated by a bracket (]), with flanking markers shown in boldface. Marker map order and position are based on the Généthon and Marshfield human sex-averaged linkage maps. The approximate location of EMP2, based on previous radiation hybrid mapping, is indicated by a brace (}). The American Journal of Human Genetics 2002 70, 244-250DOI: (10.1086/337943) Copyright © 2002 The American Society of Human Genetics Terms and Conditions