E. YÜCEL, "Congenital neutropenia caused by an autosomal recessive loss of function mutation in SMARCD2," The Joint Işıl Berat Barlan Symposium on Immunologic Disorders and The History of Medicine Meeting along with USERN Congress 2021 , İstanbul, Turkey, 2021
YÜCEL, E. 2021. Congenital neutropenia caused by an autosomal recessive loss of function mutation in SMARCD2. The Joint Işıl Berat Barlan Symposium on Immunologic Disorders and The History of Medicine Meeting along with USERN Congress 2021 , (İstanbul, Turkey).
YÜCEL, E., (2021). Congenital neutropenia caused by an autosomal recessive loss of function mutation in SMARCD2 . The Joint Işıl Berat Barlan Symposium on Immunologic Disorders and The History of Medicine Meeting along with USERN Congress 2021, İstanbul, Turkey
YÜCEL, Esra. "Congenital neutropenia caused by an autosomal recessive loss of function mutation in SMARCD2," The Joint Işıl Berat Barlan Symposium on Immunologic Disorders and The History of Medicine Meeting along with USERN Congress 2021, İstanbul, Turkey, 2021
YÜCEL, Esra. "Congenital neutropenia caused by an autosomal recessive loss of function mutation in SMARCD2." The Joint Işıl Berat Barlan Symposium on Immunologic Disorders and The History of Medicine Meeting along with USERN Congress 2021 , İstanbul, Turkey, 2021
YÜCEL, E. (2021) . "Congenital neutropenia caused by an autosomal recessive loss of function mutation in SMARCD2." The Joint Işıl Berat Barlan Symposium on Immunologic Disorders and The History of Medicine Meeting along with USERN Congress 2021 , İstanbul, Turkey.
@conferencepaper{conferencepaper, author={Esra YÜCEL}, title={Congenital neutropenia caused by an autosomal recessive loss of function mutation in SMARCD2}, congress name={The Joint Işıl Berat Barlan Symposium on Immunologic Disorders and The History of Medicine Meeting along with USERN Congress 2021}, city={İstanbul}, country={Turkey}, year={2021}}