1. Two reciprocal translocations associated with microcephaly and retardation;Bell, E.F.; Warburton, D.;Journal of Medical Genetics,1977
2. Balanced t(8; 9) (ql2; q33)pat carrier with phenotypic abnormalities attributable to a de novo terminal deletion of the long arm;Biederman, B.; Bowen, P.,1978
3. Double translocation t(7; 12), t(2; 6) heterozygosity in one family;Bijlsma, J.B.; de France, H.F.; Bleeker-Wagemakers, L.M.; Dijkstra, P.F.;Human Genetics,1978
4. Complex translocation t(9; 21) (9; 22) (ql2; pl3) (ql2; ql 1) in thefamily of a child with 9ptrisomysyndrome;Dallapiccola, B.; Bollea, G.; Mazzilli, C.; Gandini, E.;Human Genetics,1976
5. Deux translocations familiales survenues ensemble chez chacune de deux soeurs, l'une equilibree, I'autre trisomique partielle 10q;de Grouchy, J.; Finaz, C.; Roubin, M.; Roy, J.;Annales de GeWndtique,1972