1. A cluster of cystic fibrosis mutations in exon 17b of the CFTR gene: a site for rare mutations. Issue 9 (September 1994) Authors: Mercier, B; Lissens, W; Novelli, G; Kalaydjieva, L; de Arce, M; Kapranov, N; Canki Klain, N; Estivill, X; Palacio, A; Cashman, S Journal: Journal of medical genetics Issue: Volume 31:Issue 9(1994) Page Start: 731 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A novel Gypsy founder mutation, p.Arg1109X in the CMT4C gene, causes variable peripheral neuropathy phenotypes. Issue 12 (2nd December 2005) Authors: Gooding, R; Colomer, J; King, R; Angelicheva, D; Marns, L; Parman, Y; Chandler, D; Bertranpetit, J; Kalaydjieva, L Journal: Journal of medical genetics Issue: Volume 42:Issue 12(2005) Page Start: e69 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Classical phenylketonuria in Bulgaria: RFLP haplotypes and frequency of the major mutations. Issue 12 (December 1990) Authors: Kalaydjieva, L; Dworniczak, B; Aulehla-Scholz, C; Kremensky, I; Bronzova, J; Eigel, A; Horst, J Journal: Journal of medical genetics Issue: Volume 27:Issue 12(1990) Page Start: 742 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Cystic fibrosis in Bulgaria. Issue 11 (November 1991) Authors: Kalaydjieva, L; Angelicheva, D; Galeva, I; Lalov, V; Konstantinova, D Journal: Journal of medical genetics Issue: Volume 28:Issue 11(1991) Page Start: 807 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Screening for phenylketonuria in a totalitarian state. Issue 9 (September 1992) Authors: Kalaydjieva, L; Kremensky, I Journal: Journal of medical genetics Issue: Volume 29:Issue 9(1992) Page Start: 656 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Silent mutations in the phenylalanine hydroxylase gene as an aid to the diagnosis of phenylketonuria. Issue 10 (October 1991) Authors: Kalaydjieva, L; Dworniczak, B; Aulehla-Scholz, C; Devoto, M; Romeo, G; Sturhmann, M; Kucinskas, V; Yurgelyavicius, V; Horst, J Journal: Journal of medical genetics Issue: Volume 28:Issue 10(1991) Page Start: 686 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. The molecular basis of beta thalassaemia in Bulgaria. Issue 10 (October 1989) Authors: Kalaydjieva, L; Eigel, A; Horst, J Journal: Journal of medical genetics Issue: Volume 26:Issue 10(1989) Page Start: 614 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗