1. Duplications in addition to terminal deletions are present in a proportion of ring chromosomes: clues to the mechanisms of formation. Issue 3 (15th November 2007) Authors: Rossi, E; Riegel, M; Messa, J; Gimelli, S; Maraschio, P; Ciccone, R; Stroppi, M; Riva, P; Perrotta, C S; Mattina, T; Memo, L; Baumer, A; Kucinskas, V; Castellan, C; Schinzel, A; Zuffardi, O Journal: Journal of medical genetics Issue: Volume 45:Issue 3(2008) Page Start: 147 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Germline MSH2 and MLH1 mutational spectrum in HNPCC families from Poland and the Baltic States. Issue 10 (1st October 2002) Authors: Kurzawski, G; Suchy, J; Kładny, J; Safranow, K; Jakubowska, A; Elsakov, P; Kucinskas, V; Gardovski, J; Irmejs, A; Sibul, H; Huzarski, T; Byrski, T; Dębniak, T; Cybulski, C; Gronwald, J; Oszurek, O; Clark, J; Góźdź, S; Niepsuj, S; Słomski, R Journal: Journal of medical genetics Issue: Volume 39:Issue 10(2002) Page Start: e65 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Silent mutations in the phenylalanine hydroxylase gene as an aid to the diagnosis of phenylketonuria. Issue 10 (October 1991) Authors: Kalaydjieva, L; Dworniczak, B; Aulehla-Scholz, C; Devoto, M; Romeo, G; Sturhmann, M; Kucinskas, V; Yurgelyavicius, V; Horst, J Journal: Journal of medical genetics Issue: Volume 28:Issue 10(1991) Page Start: 686 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗