Precise Genetic Mapping and Haplotype Analysis of the Familial Dysautonomia Gene on Human Chromosome 9q31  Anat Blumenfeld, Susan A. Slaugenhaupt, Christopher.

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Precise Genetic Mapping and Haplotype Analysis of the Familial Dysautonomia Gene on Human Chromosome 9q31  Anat Blumenfeld, Susan A. Slaugenhaupt, Christopher B. Liebert, Violeta Temper, Channa Maayan, Sandra Gill, Diane E. Lucente, Maria Idelson, Kathy MacCormack, Mary Anne Monahan, James Mull, Maire Leyne, Marc Mendillo, Taryn Schiripo, Esther Mishori, Xandra Breakefield, Felicia B. Axelrod, James F. Gusella  The American Journal of Human Genetics  Volume 64, Issue 4, Pages 1110-1118 (April 1999) DOI: 10.1086/302339 Copyright © 1999 The American Society of Human Genetics Terms and Conditions

Figure 1 FD pedigrees showing recombination events that define the candidate interval. A, Centromeric cross. B, Telomeric cross. Blackened bars represent FD chromosomes, and unblackened bars represent non-FD chromosomes. The horizontal lines show the locations of the recombination events. The American Journal of Human Genetics 1999 64, 1110-1118DOI: (10.1086/302339) Copyright © 1999 The American Society of Human Genetics Terms and Conditions

Figure 2 Extended haplotype analysis of 435 FD chromosomes, with nine markers. The major haplotype is across the top of the box. The other haplotypes, which are believed to be derived from ancestral recombination events, are depicted, with the identical FD core markers outlined. The American Journal of Human Genetics 1999 64, 1110-1118DOI: (10.1086/302339) Copyright © 1999 The American Society of Human Genetics Terms and Conditions