Cg. Mullighan et al., HIGH-RESOLUTION HLA-DQB1 TYPING USING THE POLYMERASE CHAIN-REACTION AND SEQUENCE-SPECIFIC PRIMERS, Tissue antigens, 50(6), 1997, pp. 688-692
Polymorphism at HLA-DQB1 is known to influence tissue compatibility an
d disease susceptibility; however, current DQB1 typing methods are una
ble to distinguish the 32 currently recognized DQB1 alleles. We have d
eveloped a 32-reaction PCR-SSP method capable of differentiating all D
QB1 alleles that differ in amino acid sequence. This method can resolv
e all heterozygous combinations of DQB1 alleles, with the exception of
several combinations involving alleles not thus far detected in Cauca
soid populations.