1. A patient with Wolf-Hirschhorn syndrome originating from translocation t(4;8) (p16.3;q24.3)pat. Issue 1 (January 1995) Authors: el-Rifai, W; Leisti, J; Kähkönen, M; Pietarinen, A; Altherr, M R; Knuutila, S Journal: Journal of medical genetics Issue: Volume 32:Issue 1(1995) Page Start: 65 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Absence of IgA and growth hormone deficiency associated with short arm deletion of chromosome 18. Issue 4 (April 1973) Authors: Leisti, J; Leisti, S; Perheentupa, J; Savilahti, E; Aula, P Journal: Archives of disease in childhood Issue: Volume 48:Issue 4(1973) Page Start: 320 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Hereditary spinal neurofibromatosis: a rare form of NF1?. Issue 3 (March 1997) Authors: Poyhonen, M; Leisti, E L; Kytölä, S; Leisti, J Journal: Journal of medical genetics Issue: Volume 34:Issue 3(1997) Page Start: 184 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Lethal congenital contracture syndrome (LCCS), a fetal anterior horn cell disease, is not linked to the SMA 5q locus. Issue 1 (January 1995) Authors: Vuopala, K; Mäkelä-Bengs, P; Suomalainen, A; Herva, R; Leisti, J; Peltonen, L Journal: Journal of medical genetics Issue: Volume 32:Issue 1(1995) Page Start: 36 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Myotonia congenita in northern Finland: an epidemiological and genetic study. Issue 4 (April 1998) Authors: Baumann, P; Myllylä, V V; Leisti, J Journal: Journal of medical genetics Issue: Volume 35:Issue 4(1998) Page Start: 293 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. New lethal disease involving type I and III collagen defect resembling geroderma osteodysplastica, De Barsy syndrome, and Ehlers-Danlos syndrome IV. Issue 6 (June 1998) Authors: Jukkola, A; Kauppila, S; Risteli, L; Vuopala, K; Risteli, J; Leisti, J; Pajunen, L Journal: Journal of medical genetics Issue: Volume 35:Issue 6(1998) Page Start: 513 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Northern epilepsy syndrome: an inherited childhood onset epilepsy with associated mental deterioration. Issue 3 (March 1994) Authors: Hirvasniemi, A; Lang, H; Lehesjoki, A E; Leisti, J Journal: Journal of medical genetics Issue: Volume 31:Issue 3(1994) Page Start: 177 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Two chromosome fragments in a child with Down's syndrome and transient chromosome aberrations in the mother. Issue 3 (June 1983) Authors: Knuutila, S; Leisti, J; Salunen, R; Rossi, L Journal: Journal of medical genetics Issue: Volume 20:Issue 3(1983) Page Start: 232 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗