T. Shahin Et Al. , "Selective loss of function variants in IL6ST cause Hyper-IgE syndrome with distinct impairments of T-cell phenotype and function," HAEMATOLOGICA , vol.104, no.3, pp.609-621, 2019
Shahin, T. Et Al. 2019. Selective loss of function variants in IL6ST cause Hyper-IgE syndrome with distinct impairments of T-cell phenotype and function. HAEMATOLOGICA , vol.104, no.3 , 609-621.
Shahin, T., Aschenbrenner, D., Cagdas, D., Bal, S. K., Conde, C. D., Garncarz, W., ... Medgyesi, D.(2019). Selective loss of function variants in IL6ST cause Hyper-IgE syndrome with distinct impairments of T-cell phenotype and function. HAEMATOLOGICA , vol.104, no.3, 609-621.
Shahin, DENİZ Et Al. "Selective loss of function variants in IL6ST cause Hyper-IgE syndrome with distinct impairments of T-cell phenotype and function," HAEMATOLOGICA , vol.104, no.3, 609-621, 2019
Shahin, DENİZ N. Et Al. "Selective loss of function variants in IL6ST cause Hyper-IgE syndrome with distinct impairments of T-cell phenotype and function." HAEMATOLOGICA , vol.104, no.3, pp.609-621, 2019
Shahin, T. Et Al. (2019) . "Selective loss of function variants in IL6ST cause Hyper-IgE syndrome with distinct impairments of T-cell phenotype and function." HAEMATOLOGICA , vol.104, no.3, pp.609-621.
@article{article, author={DENİZ NAZİRE ÇAĞDAŞ AYVAZ Et Al. }, title={Selective loss of function variants in IL6ST cause Hyper-IgE syndrome with distinct impairments of T-cell phenotype and function}, journal={HAEMATOLOGICA}, year=2019, pages={609-621} }