1. Quinacrine mustard fluorescence of human chromosomes: characterization of unusual translocations;l Francke U;Am J Hum Genet,1972
2. Trisomie 10 partielle par translocation familiale t(1; 10)(q44; q22);Laurent, C.; Bovier-Lapierre, M.; Dutrillaux, B.;Humangenetik,1973
3. Sanchez 0. A new syndrome resulting from partial trisomy for the distal third of the long arm of chromosome 10;Yunis, J.J.;J Pediatr,1974
4. Malformation syndrome of chromosome 10q duplication and the Vater association;Field, B.; Smith, A.; Sillence, D.;Ann Genet (Paris),1983
5. Familial partial trisomy 10q(q23-.qter) syndrome and paracentric inversion 3(q31q26) in the same patient;Bass, H.N.; Sparkes, R.S.; Crandall, B.F.; Tannenbaum, S.M.;Ann Genet (Paris),1978