D. Kancheva Et Al. , "Novel mutations in genes causing hereditary spastic paraplegia and Charcot-Marie-Tooth neuropathy identified by an optimized protocol for homozygosity mapping based on whole-exome sequencing," GENETICS IN MEDICINE , vol.18, no.6, pp.600-607, 2016
Kancheva, D. Et Al. 2016. Novel mutations in genes causing hereditary spastic paraplegia and Charcot-Marie-Tooth neuropathy identified by an optimized protocol for homozygosity mapping based on whole-exome sequencing. GENETICS IN MEDICINE , vol.18, no.6 , 600-607.
Kancheva, D., Atkinson, D., De Rijk, P., Zimon, M., Chamova, T., Mitev, V., ... YARAMIŞ, A.(2016). Novel mutations in genes causing hereditary spastic paraplegia and Charcot-Marie-Tooth neuropathy identified by an optimized protocol for homozygosity mapping based on whole-exome sequencing. GENETICS IN MEDICINE , vol.18, no.6, 600-607.
Kancheva, Daliya Et Al. "Novel mutations in genes causing hereditary spastic paraplegia and Charcot-Marie-Tooth neuropathy identified by an optimized protocol for homozygosity mapping based on whole-exome sequencing," GENETICS IN MEDICINE , vol.18, no.6, 600-607, 2016
Kancheva, Daliya Et Al. "Novel mutations in genes causing hereditary spastic paraplegia and Charcot-Marie-Tooth neuropathy identified by an optimized protocol for homozygosity mapping based on whole-exome sequencing." GENETICS IN MEDICINE , vol.18, no.6, pp.600-607, 2016
Kancheva, D. Et Al. (2016) . "Novel mutations in genes causing hereditary spastic paraplegia and Charcot-Marie-Tooth neuropathy identified by an optimized protocol for homozygosity mapping based on whole-exome sequencing." GENETICS IN MEDICINE , vol.18, no.6, pp.600-607.
@article{article, author={Daliya Kancheva Et Al. }, title={Novel mutations in genes causing hereditary spastic paraplegia and Charcot-Marie-Tooth neuropathy identified by an optimized protocol for homozygosity mapping based on whole-exome sequencing}, journal={GENETICS IN MEDICINE}, year=2016, pages={600-607} }