1. "Molecular rulers" for calibrating phenotypic effects of telomere imbalance. Issue 10 (1st October 2002) Authors: Martin, C L; Waggoner, D J; Wong, A; Uhrig, S; Roseberry, J A; Hedrick, J F; Pack, S D; Russell, K; Zackai, E; Dobyns, W B; Ledbetter, D H Journal: Journal of medical genetics Issue: Volume 39:Issue 10(2002) Page Start: 734 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. "New microdeletion syndromes: complex, but no new paradigms". Issue 8 (31st July 2009) Authors: Ledbetter, D H Journal: Journal of medical genetics Issue: Volume 46:Issue 8(2009) Page Start: 576 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Analysis of parent of origin specific DNA methylation at SNRPN and PW71 in tissues: implication for prenatal diagnosis. Issue 12 (December 1996) Authors: Kubota, T; Aradhya, S; Macha, M; Smith, A C; Surh, L C; Satish, J; Verp, M S; Nee, H L; Johnson, A; Christan, S L; Ledbetter, D H Journal: Journal of medical genetics Issue: Volume 33:Issue 12(1996) Page Start: 1011 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Classical lissencephaly syndromes: does the face reflect the brain?. Issue 11 (November 1998) Authors: Allanson, J E; Ledbetter, D H; Dobyns, W B Journal: Journal of medical genetics Issue: Volume 35:Issue 11(1998) Page Start: 920 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Miller-Dieker syndrome resulting from rearrangement of a familial chromosome 17 inversion detected by fluorescence in situ hybridisation. Issue 1 (January 1996) Authors: Kingston, H M; Ledbetter, D H; Tomlin, P I; Gaunt, K L Journal: Journal of medical genetics Issue: Volume 33:Issue 1(1996) Page Start: 69 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Molecular screening for proximal 15q abnormalities in a mentally retarded population. Issue 7 (July 1998) Authors: Jacobsen, J; King, B H; Leventhal, B L; Christian, S L; Ledbetter, D H; Cook, E H Journal: Journal of medical genetics Issue: Volume 35:Issue 7(1998) Page Start: 534 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Organisation of the pericentromeric region of chromosome 15: at least four partial gene copies are amplified in patients with a proximal duplication of 15q. Issue 3 (1st March 2002) Authors: Fantes, J A; Mewborn, S K; Lese, C M; Hedrick, J; Brown, R L; Dyomin, V; Chaganti, R S K; Christian, S L; Ledbetter, D H Journal: Journal of medical genetics Issue: Volume 39:Issue 3(2002) Page Start: 170 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Subtelomere FISH analysis of 11 688 cases: an evaluation of the frequency and pattern of subtelomere rearrangements in individuals with developmental disabilities. Issue 6 (30th September 2005) Authors: Ravnan, J B; Tepperberg, J H; Papenhausen, P; Lamb, A N; Hedrick, J; Eash, D; Ledbetter, D H; Martin, C L Journal: Journal of medical genetics Issue: Volume 43:Issue 6(2006) Page Start: 478 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Two 22q telomere deletions serendipitously detected by FISH. Issue 11 (November 1998) Authors: Precht, K S; Lese, C M; Spiro, R P; Huttenlocher, P R; Johnston, K M; Baker, J C; Christian, S L; Kittikamron, K; Ledbetter, D H Journal: Journal of medical genetics Issue: Volume 35:Issue 11(1998) Page Start: 939 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗