Figure 2 of Qin, Mol Vis 2006; 12:1001-1008.


Figure 2.

Haplotype analysis of the WS1 family using chromosome 2 markers. Sequence of markers is D2s364, D2s117, D2S325, D2S2382, D2S2248, D2S126, D2S396, and D2S206 from centromere to telomere. Blackened bars indicate the affected haplotype. Recombination events seen place the disease gene locus to a 45.74 cM region between markers D2S117 and D2S206.

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Qin, Mol Vis 2006; 12:1001-1008 <http://www.molvis.org/molvis/v12/a112/>
©2006 Molecular Vision <http://www.molvis.org/molvis/>
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