BİŞGİN, A. Et Al. 2021. The evaluation of rare and low-frequency genetic variants in common variable immune deficiency (CVID) patients together with CV/RVCD (common variant/rare variant, common disease) hypothesis for final interpretation. 6. Uluslararası Katılımlı Erciyes Tıp Tibbi Genetik Kongresi , (Turkey).

BİŞGİN, A., SÖNMEZLER, Ö., BOGA, İ., & YILMAZ, M., (2021). The evaluation of rare and low-frequency genetic variants in common variable immune deficiency (CVID) patients together with CV/RVCD (common variant/rare variant, common disease) hypothesis for final interpretation . 6. Uluslararası Katılımlı Erciyes Tıp Tibbi Genetik Kongresi, Turkey

BİŞGİN, ATIL Et Al. "The evaluation of rare and low-frequency genetic variants in common variable immune deficiency (CVID) patients together with CV/RVCD (common variant/rare variant, common disease) hypothesis for final interpretation," 6. Uluslararası Katılımlı Erciyes Tıp Tibbi Genetik Kongresi, Turkey, 2021

BİŞGİN, ATIL Et Al. "The evaluation of rare and low-frequency genetic variants in common variable immune deficiency (CVID) patients together with CV/RVCD (common variant/rare variant, common disease) hypothesis for final interpretation." 6. Uluslararası Katılımlı Erciyes Tıp Tibbi Genetik Kongresi , Turkey, 2021

BİŞGİN, A. Et Al. (2021) . "The evaluation of rare and low-frequency genetic variants in common variable immune deficiency (CVID) patients together with CV/RVCD (common variant/rare variant, common disease) hypothesis for final interpretation." 6. Uluslararası Katılımlı Erciyes Tıp Tibbi Genetik Kongresi , Turkey.

@conferencepaper{conferencepaper, author={ATIL BİŞGİN Et Al. }, title={The evaluation of rare and low-frequency genetic variants in common variable immune deficiency (CVID) patients together with CV/RVCD (common variant/rare variant, common disease) hypothesis for final interpretation}, congress name={6. Uluslararası Katılımlı Erciyes Tıp Tibbi Genetik Kongresi}, city={}, country={Turkey}, year={2021}}