1. A single origin for the most frequent mutation causing late infantile metachromatic leucodystrophy. Issue 9 (September 1994) Authors: Zlotogora, J; Furman-Shaharabani, Y; Harris, A; Barth, M L; von Figura, K; Gieselmann, V Journal: Journal of medical genetics Issue: Volume 31:Issue 9(1994) Page Start: 672 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Frequency of arylsulphatase A pseudodeficiency associated mutations in a healthy population. Issue 9 (September 1994) Authors: Barth, M L; Ward, C; Harris, A; Saad, A; Fensom, A Journal: Journal of medical genetics Issue: Volume 31:Issue 9(1994) Page Start: 667 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Gaucher's disease in the United Kingdom: screening non-Jewish patients for the two common mutations. Issue 4 (April 1993) Authors: Walley, A J; Barth, M L; Ellis, I; Fensom, A H; Harris, A Journal: Journal of medical genetics Issue: Volume 30:Issue 4(1993) Page Start: 280 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. The arylsulphatase A gene and molecular genetics of metachromatic leucodystrophy. Issue 9 (September 1994) Authors: Barth, M L; Fensom, A; Harris, A Journal: Journal of medical genetics Issue: Volume 31:Issue 9(1994) Page Start: 663 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Very low levels of high density lipoprotein cholesterol in four sibs of a family with non-neuropathic Niemann-Pick disease and sea-blue histiocytosis. Issue 8 (August 1990) Authors: Viana, M B; Giugliani, R; Leite, V H; Barth, M L; Lekhwani, C; Slade, C M; Fensom, A Journal: Journal of medical genetics Issue: Volume 27:Issue 8(1990) Page Start: 499 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗