Osteoarthrosis (OA) is a major component of many osteochondrodysplasti
c syndromes which follow mendelian modes of inheritance. The use of mo
lecular genetic techniques to unravel the molecular background of OA h
as therefore become possible. Linkage analysis, positional cloning, an
d candidate gene analysis have been used to identify genes which, when
altered, can lead to syndromic OA. Allele association studies and sib
-pair analysis have also made it possible to study the importance of a
particular gene or locus in OA at the population level. Furthermore,
the creation of transgenic mice and analyses of naturally occurring an
d chemically or radiologically induced mutations in mice are providing
in vivo models for human osteochondrodysplasias and OA.