Figure 5. Pedigree and haplotype analysis
of family XT at the FEOM1 and FEOM3 loci. Black symbols identify
clinically affected individuals. Genotyping data and schematic
haplotype bars for FEOM1 markers (A) and FEOM3 markers (B)
are
shown below the symbol for each individual. The black bars denote
the potential disease-associated alleles. The white bars indicate the
inheritance of non disease-associated haplotypes.
Yang, Mol Vis 2010; 16:2062-2070. http://www.molvis.org/molvis/v16/a222
©2010 Molecular Vision http://www.molvis.org/molvis/
ISSN 1090-0535