1. 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) ↗
2. Inheritance of the fragile X syndrome: size of the fragile X premutation is a major determinant of the transition to full mutation. Issue 11 (November 1992) Authors: Heitz, D; Devys, D; Imbert, G; Kretz, C; Mandel, J L Journal: Journal of medical genetics Issue: Volume 29:Issue 11(1992) Page Start: 794 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Selection in blood cells from female carriers of the fragile X syndrome: inverse correlation between age and proportion of active X chromosomes carrying the full mutation. Issue 12 (December 1991) Authors: Rousseau, F; Heitz, D; Oberlé, I; Mandel, J L Journal: Journal of medical genetics Issue: Volume 28:Issue 12(1991) Page Start: 830 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗