1. A single base alteration in the CGG repeat region of FMR1: possible effects on gene expression and phenotype. Issue 3 (1st March 2002) Authors: Tarleton, J; Kenneson, A; Taylor, A K; Crandall, K; Fletcher, R; Casey, R; Hart, P S; Hatton, D; Fisch, G; Warren, S T Journal: Journal of medical genetics Issue: Volume 39:Issue 3(2002) Page Start: 196 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Difficult diagnosis of the fragile X syndrome made possible by direct detection of DNA mutations. Issue 10 (October 1992) Authors: Tarleton, J; Wong, S; Heitz, D; Schwartz, C Journal: Journal of medical genetics Issue: Volume 29:Issue 10(1992) Page Start: 726 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Direct analysis of the FMR-1 gene provides an explanation for an exceptional case of a fragile X negative, mentally retarded male in a fragile X family. Issue 12 (December 1992) Authors: Tarleton, J; Wong, S; Schwartz, C Journal: Journal of medical genetics Issue: Volume 29:Issue 12(1992) Page Start: 919 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. The elusive Angelman syndrome critical region. Issue 9 (September 1997) Authors: Trent, R J; Sheffield, L J; Deng, Z M; Kim, W S; Nassif, N T; Ryce, C; Woods, C G; Michaelis, R C; Tarleton, J; Smith, A Journal: Journal of medical genetics Issue: Volume 34:Issue 9(1997) Page Start: 714 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗