BioMed Research International / 2011 / Article / Fig 1

Research Article

Identification of Missense Mutation (I12T) in the BSND Gene and Bioinformatics Analysis

Figure 1

Pedigree of family with nonsyndromic autosomal recessive hearing loss associated haplotypes. Haplotypes for the most closely linked STRPs are shown below each symbol. The genetic map distances according to the Marshfield genetic map in centimorgans (cM) are shown in parenthesis next to the marker name. Arrows adjacent to the haplotypes indicate key recombination events. The alleles are denoted 1–3 according to their allele size.
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