1. Diversity of the basic defect of homozygous CFTR mutation genotypes in humans. Issue 1 (4th January 2008) Authors: Stanke, F; Ballmann, M; Bronsveld, I; Dörk, T; Gallati, S; Laabs, U; Derichs, N; Ritzka, M; Posselt, H-G; Harms, H K; Griese, M; Blau, H; Mastella, G; Bijman, J; Veeze, H; Tümmler, B Journal: Journal of medical genetics Issue: Volume 45:Issue 1(2008) Page Start: 47 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Professor McNeish and co-workers comment. Issue 7 (July 1980) Authors: McNeish, A S; Harms, H K; Rey, J; Shmerling, D H; Visakorpi, J K; Walker-Smith, J A Journal: Archives of disease in childhood Issue: Volume 55:Issue 7(1980) Page Start: 576 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. The diagnosis of coeliac disease. A commentary on the current practices of members of the European Society for Paediatric Gastroenterology and Nutrition (ESPGAN). Issue 10 (October 1979) Authors: McNeish, A S; Harms, H K; Rey, J; Shmerling, D H; Visakorpi, J K; Walker-Smith, J A Journal: Archives of disease in childhood Issue: Volume 54:Issue 10(1979) Page Start: 783 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗