1. Partial trisomy 14qand parental translocation of No 14 chromosome;Simpson, J.; Zellweger, H.;J Med Genet; arose at maternal oogenesis by 3: 1 disjunction at the first meiotic division, the segregation resulting in the normal chromosomes 3 and 14 and the 14qfragment moving to the same pole at anaphase I,1977
2. Familial partial 14 trisomy;Miller, J.Q.; Willson, K.; Wyandt, H.; Jaramillo, M.A.; McConnell, T.S.;J Med Genet,1979
3. A simple method for R banding of human we do not know if the translocation arose in the mother de novo, or was inherited from her father (who was dead). It would seem likely that the translocation arose de novo in the mother as none of chromosomes, showing a pH dependent connection between R;Sehested, J.,1974
4. Localisation of heterochromatin in human chromosomes;Arrighi, F.E.; Hsu, T.C.;Cytogenetics,1971
5. Gendel her sibs carried it, which would be unusual if the father was a carrier. Other families reported in which an unbalanced proband had arisen by 3: 1 disjunction from a carrier mother showed many E, Zelson C. Familial translocation involving chromosomes 6, 14 and 20, identified by quinacrine fluorescence;Allderdice, P.W.; Miller, O.J.; Miller, D.A.; Breg, W.R.;Hum Genet; Clinical atlas ofhuman chromosomes,1971