1. Molecular studies in Finnish patients with familial juvenile nephronophthisis exclude a founder effect and support a common mutation causing mechanism. Issue 4 (April 1998) Authors: Ala-Mello, S; Sankila, E M; Koskimies, O; de la Chapelle, A; Kääriäinen, H Journal: Journal of medical genetics Issue: Volume 35:Issue 4(1998) Page Start: 279 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. X linked neonatal myotubular myopathy: one recombination detected with four polymorphic DNA markers from Xq28. Issue 5 (May 1990) Authors: Lehesjoki, A E; Sankila, E M; Miao, J; Somer, M; Salonen, R; Rapola, J; de la Chapelle, A Journal: Journal of medical genetics Issue: Volume 27:Issue 5(1990) Page Start: 288 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗