1. Localisation of a gene for transient neonatal diabetes mellitus to an 18.72 cR3000 (∼5.4 Mb) interval on chromosome 6q. Issue 3 (1st March 1999) Authors: Gardner, Rebecca J; Mungall, Andrew J; Dunham, Ian; Barber, John C K; Shield, Julian P H; Temple, I Karen; Robinson, David O Journal: Journal of medical genetics Issue: Volume 36:Issue 3(1999) Page Start: 192 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Medical genetics: advances in brief. Issue 1 (January 1998) Authors: Robinson, David O Journal: Journal of medical genetics Issue: Volume 35:Issue 1(1998) Page Start: 81 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Medical genetics: advances in brief. Issue 11 (November 1997) Authors: Robinson, David O Journal: Journal of medical genetics Issue: Volume 34:Issue 11(1997) Page Start: 957 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Medical genetics: advances in brief. Issue 8 (August 1997) Authors: Robinson, David O Journal: Journal of medical genetics Issue: Volume 34:Issue 8(1997) Page Start: 700 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Medical genetics: advances in brief: An activating splice donor mutation in the thrombopoietin gene causes hereditary thrombocythaemia. Issue 6 (June 1998) Authors: Robinson, David O Journal: Journal of medical genetics Issue: Volume 35:Issue 6(1998) Page Start: 525 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Medical genetics: advances in brief: Functional screening of 2 Mb of human chromosome 21q22.2 in transgenic mice implicates minibrain in learning defects associated with Down syndrome. Issue 9 (September 1997) Authors: Robinson, David O Journal: Journal of medical genetics Issue: Volume 34:Issue 9(1997) Page Start: 787 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Medical genetics: advances in brief: Mutations in GLUT2, the gene for the liver type glucose transporter, in patients with Fanconi-Bickel syndrome. Issue 4 (April 1998) Authors: Robinson, David O Journal: Journal of medical genetics Issue: Volume 35:Issue 4(1998) Page Start: 345 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Medical genetics: advances in brief: Mutations in the caveolin-3 gene cause autosomal dominant limb-girdle muscular dystrophy. Issue 9 (September 1998) Authors: Robinson, David O Journal: Journal of medical genetics Issue: Volume 35:Issue 9(1998) Page Start: 787 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Medical genetics: advances in brief: Positional cloning of the gene associated with X-linked juvenile retinoschisis. Issue 3 (March 1998) Authors: Robinson, David O Journal: Journal of medical genetics Issue: Volume 35:Issue 3(1998) Page Start: 261 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Medical genetics: advances in brief: Role of the region 3' to Xist exon 6 in the counting process of X-chromosome inactivation. Issue 11 (November 1998) Authors: Robinson, David O Journal: Journal of medical genetics Issue: Volume 35:Issue 11(1998) Page Start: 961 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗