Skip to main content
. 2010 Jul 13;11(4):449–455. doi: 10.1007/s10048-010-0250-9

Fig. 1.

Fig. 1

Pedigrees of 13 families with autosomal recessive muscular dystrophy or myopathy. Squares males, circles females, filled symbols affected individuals, partially black-filled symbols obligate heterozygous carriers, partially gray-filled symbols possible heterozygous carriers, open symbols unaffected individuals. Double bars represent consanguineous unions. Asterisks denote individuals genotyped for genomewide linkage analysis