Figure 1.
Pedigrees Harboring Subjects with the Autosomal-Recessive Phenotype Syndactyly Type IX, Mesoaxial Synostotic Syndactyly, Malik-Percin Type
For clarity, pedigrees have been trimmed. Extended pedigrees for families 1 and 2 have been reported previously.1,3 Black symbols indicate clinically affected individuals. Haplotypes for the microsatellite markers from the candidate interval at chromosome 17p13.3 genotyped in family 3 are depicted. The autozygous region segregating in the affected subjects is given in shaded block. A minus sign (−) shows the alleles that could not be genotyped. BHLHA9 missense mutations segregating in the families are indicated.