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. Author manuscript; available in PMC: 2014 Mar 1.
Published in final edited form as: Clin Genet. 2012 Jun 4;83(3):238–243. doi: 10.1111/j.1399-0004.2012.01898.x

Fig. 1.

Fig. 1

Genotype data spanning the PMS2 locus in probands carrying mutations c.137G>T, exon 10 deletion, c.903G>T or c.1A>G. The alleles associated with the mutation are bolded and the shared haplotypes are represented by the empty bars.

*the samples from the ARUP Laboratories; **frequencies in controls of the bolded alleles.