Tuysuz, B. Et Al. 2016. Phenotypic Expansion of Congenital Disorder of Glycosylation Due to SRD5A3 Null Mutation.. JIMD reports , vol.26 , 7-12.

Tuysuz, B., PEHLIVAN, D., ÖZKÖK, A., JHANGIANI, S., YALCINKAYA, C., ZEYBEK, Ç., ... MUZNY, D.(2016). Phenotypic Expansion of Congenital Disorder of Glycosylation Due to SRD5A3 Null Mutation.. JIMD reports , vol.26, 7-12.

Tuysuz, Beyhan Et Al. "Phenotypic Expansion of Congenital Disorder of Glycosylation Due to SRD5A3 Null Mutation.," JIMD reports , vol.26, 7-12, 2016

Tuysuz, Beyhan Et Al. "Phenotypic Expansion of Congenital Disorder of Glycosylation Due to SRD5A3 Null Mutation.." JIMD reports , vol.26, pp.7-12, 2016

Tuysuz, B. Et Al. (2016) . "Phenotypic Expansion of Congenital Disorder of Glycosylation Due to SRD5A3 Null Mutation.." JIMD reports , vol.26, pp.7-12.

@article{article, author={Beyhan TÜYSÜZ Et Al. }, title={Phenotypic Expansion of Congenital Disorder of Glycosylation Due to SRD5A3 Null Mutation.}, journal={JIMD reports}, year=2016, pages={7-12} }