1. Familial translocation involving chromosomes 6, 14 and 20, identified by quinacrine fluorescence;Humangenetik,1971
2. An inherited translocation t(4; 15) (p16; q22) leading to two cases of;Cohen, M.M.; Ornoy, A.; Rosenmann, A.; Kohn, G.;partial trisomy 15. Annals de Genetique,1975
3. Pachytene analysis in a human reciprocal (10; 11) translocation;Ferguson-Smith, M.A.; Page, B.M.;Journal of Medical Genetics,1973
4. Quinacrine mustard fluorescence of human chromosomes: characterization of unusual translocations;Francke, U.;American Joiurnal ofHuman Genetics,1972
5. Fryns, J. P., Cassiman, J. J., and Van den Berghe, H. (1974). Tertiary partial 14 trisomy 47,XX, + 14q-. Humangenetik, 24,71-77.