1. A novel locus for autosomal dominant non-syndromic deafness (DFNA41) maps to chromosome 12q24-qter. Issue 8 (1st August 2002) Authors: Blanton, S H; Liang, C Y; Cai, M W; Pandya, A; Du, L L; Landa, B; Mummalanni, S; Li, K S; Chen, Z Y; Qin, X N; Liu, Y F; Balkany, T; Nance, W E; Liu, X Z Journal: Journal of medical genetics Issue: Volume 39:Issue 8(2002) Page Start: 567 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A novel locus for autosomal dominant non-syndromic deafness, DFNA53, maps to chromosome 14q11.2-q12. Issue 2 (15th June 2005) Authors: Yan, D; Ke, X; Blanton, S H; Ouyang, X M; Pandya, A; Du, L L; Nance, W E; Liu, X Z Journal: Journal of medical genetics Issue: Volume 43:Issue 2(2006) Page Start: 170 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. An exclusion map of Marfan syndrome. Issue 2 (February 1990) Authors: Blanton, S H; Sarfarazi, M; Eiberg, H; de Groote, J; Farndon, P A; Kilpatrick, M W; Child, A H; Pope, F M; Peltonen, L; Francomano, C A Journal: Journal of medical genetics Issue: Volume 27:Issue 2(1990) Page Start: 73 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. DTDST mutations are not a frequent cause of idiopathic talipes equinovarus (club foot). Issue 4 (1st April 2002) Authors: Bonafé, L; Blanton, S H; Scott, A; Broussard, S; Wise, C A; Superti-Furga, A; Hecht, J T Journal: Journal of medical genetics Issue: Volume 39:Issue 4(2002) Page Start: e20 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Evaluation of candidate genes for familial brachydactyly. Issue 11 (November 1995) Authors: Mastrobattista, J M; Dollé, P; Blanton, S H; Northrup, H Journal: Journal of medical genetics Issue: Volume 32:Issue 11(1995) Page Start: 851 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Exclusion of retinoic acid receptor and a cartilage matrix protein in non-syndromic CL(P) families. Issue 1 (January 1995) Authors: Stein, J D; Hecht, J T; Blanton, S H Journal: Journal of medical genetics Issue: Volume 32:Issue 1(1995) Page Start: 78 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Linkage analysis in Marfan syndrome. Issue 2 (February 1990) Authors: Schwartz, R C; Blanton, S H; Hyde, C A; Sottile, T R; Hudgins, L; Sarfarazi, M; Tsipouras, P Journal: Journal of medical genetics Issue: Volume 27:Issue 2(1990) Page Start: 86 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Report of a critical recombination further narrowing the TSC1 region. Issue 7 (July 1996) Authors: Au, K S; Murrell, J; Buckler, A; Blanton, S H; Northrup, H Journal: Journal of medical genetics Issue: Volume 33:Issue 7(1996) Page Start: 559 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗