Abstract
The major histocompatibility complex (MHC) in humans is a polymorphic assemblage of over 70 genes which play key roles in the regulation of the immune response (TROWSDALE et al. 1991). The bovine MHC (bovine lymphocyte antigen, BoLA) was assigned to a rather broad region of cattle chromosome 23 (ql3-23) by sequential Q-banding and isotopic in situ hybridization (FRIES et al. 1986; HEDIGER et al. 1991). In the present study, we use sequential RBA-banding and fluorescent in situ hybridization
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