1. Familial translocation involving chromosomes 6, 14 and 20 identified by quinacrine fluorescence;Allderdice, P.W.; Miller, O.J.; Miller, D.A.; Breg, W.R.; Gendel, E.; Lelson, C.;Humangenetik,1971
2. Trisomie 14 proximale;Faugeras, C.; Barthe, D.;Ann Pediatr (Paris),1986
3. Meiotic dysfunction in a mother with a balanced translocation, 46, XX, t(5; 14)(pl5; ql3) resulting in tertiary trisomy and tertiary monosomy offspring;Abelovich, D.; Yagupsky, P.; Bashan, N.;Am J Med Genet,1982
4. Partial trisomy 14q and familial translocation;Coco, K.K.; Penchaszadeh, V.B.P.;Ann Genet (Paris),1977
5. Partial trisomy D: a diagnostic and cytogenetic dilemma;Cohen, M.M.; Rosenmann, A.; Dagan, J.; Legum, C.;J Med Genet,1976