Table 1

Transmission disequilibrium testing results

Marker Het χ2 df p Value Primers
IL20.897.3140.12AAA GAG ACC TGC TAA CAC
TGT TTC CCC TTG CCG CC
TCF80.730.0820.96AGA GGA TCC TGT TCA CTA CTG
TGC GAA TTC TTA CTA GGT CTG AGG
D14S14190.562.3130.51TAG GGA CAG GCA GTT GAT TA
CAA TTA ATG TAA AAA TTA GCC A
D14S14200.670.7420.69TGT TTG AAG AAG GGA GTC GT
CCC ACT CCA TGT CTT CTG TT
D14S8260.741.7440.78TCT CTA AAG CTA CTA TAA CCC AG
TGC TGT TGG ACT CAG GTA GCT A
  • Each microsatellite was amplified by PCR from genomic DNA with fluorescent labelling of the forward primer and genotyped using the Applied Biosystems GENESCAN/GENOTYPER system (primers as shown in table). TDT was performed using the TRANSMIT program version 2.5, considering only those alleles with a frequency of greater than 10% (corresponding to the number of degrees of freedom {df} in the table). The chromosome 14 markers are listed in map order.

  • The families were recruited from throughout the United Kingdom. All are white and the affected offspring meet the Poser criteria, 95% having clinically definite, category A or B, disease.