T. Harel Et Al. , "Monoallelic and Biallelic Variants in EMC1 Identified in Individuals with Global Developmental Delay, Hypotonia, Scoliosis, and Cerebellar Atrophy," American Journal of Human Genetics , vol.98, no.3, pp.562-570, 2016
Harel, T. Et Al. 2016. Monoallelic and Biallelic Variants in EMC1 Identified in Individuals with Global Developmental Delay, Hypotonia, Scoliosis, and Cerebellar Atrophy. American Journal of Human Genetics , vol.98, no.3 , 562-570.
Harel, T., YEŞİL, G., Bayram, Y., Coban-Akdemir, Z., Charng, W., Karaca, E., ... Al Asmari, A.(2016). Monoallelic and Biallelic Variants in EMC1 Identified in Individuals with Global Developmental Delay, Hypotonia, Scoliosis, and Cerebellar Atrophy. American Journal of Human Genetics , vol.98, no.3, 562-570.
Harel, Tamar Et Al. "Monoallelic and Biallelic Variants in EMC1 Identified in Individuals with Global Developmental Delay, Hypotonia, Scoliosis, and Cerebellar Atrophy," American Journal of Human Genetics , vol.98, no.3, 562-570, 2016
Harel, Tamar Et Al. "Monoallelic and Biallelic Variants in EMC1 Identified in Individuals with Global Developmental Delay, Hypotonia, Scoliosis, and Cerebellar Atrophy." American Journal of Human Genetics , vol.98, no.3, pp.562-570, 2016
Harel, T. Et Al. (2016) . "Monoallelic and Biallelic Variants in EMC1 Identified in Individuals with Global Developmental Delay, Hypotonia, Scoliosis, and Cerebellar Atrophy." American Journal of Human Genetics , vol.98, no.3, pp.562-570.
@article{article, author={Tamar Harel Et Al. }, title={Monoallelic and Biallelic Variants in EMC1 Identified in Individuals with Global Developmental Delay, Hypotonia, Scoliosis, and Cerebellar Atrophy}, journal={American Journal of Human Genetics}, year=2016, pages={562-570} }