Romain D R, Columbano-Green L, Sullivan J, Smythe R H, Gebbie O, Parfitt R, Chapman C
J Med Genet. 1982 Aug;19(4):306-10. doi: 10.1136/jmg.19.4.306.
A phenotypically normal female with a history of two miscarriages was found to have the karyotype 45,XX,t(13p:13p). C banding showed the translocation to have two regions of centromeric constitutive heterochromatin, silver staining showed an active NOR in 60% of the cells screened, and Cd banding studies showed a single Cd band with absence of the Cd band at the suppressed centromere.