Rare Translocation 47, XY, t(12;21) in Down’s Syndrome

Abstract
A translocation between the long arm of chromosome 12 and the long arm of chromosome 21 was found in a male with typical Down’s syndrome. His mother and a maternal uncle carried the same translocation. Breakpoints at 12q14 and 21q22 were identified by fluorescence studies. In this family, alternate and 3-to-1 disjunctional segregation was observed.