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