S. SEYHAN Et Al. , "SNORD116 deletions cause all features of Prader-Willi syndrome," V. International Participated Erciyes Medical Genetics Days Congress , Nevşehir, Turkey, 2020
SEYHAN, S. Et Al. 2020. SNORD116 deletions cause all features of Prader-Willi syndrome. V. International Participated Erciyes Medical Genetics Days Congress , (Nevşehir, Turkey).
SEYHAN, S., AYAZ, A., Gül, D., Giriş, F. S., & CEYLANER, S., (2020). SNORD116 deletions cause all features of Prader-Willi syndrome . V. International Participated Erciyes Medical Genetics Days Congress, Nevşehir, Turkey
SEYHAN, SERHAT Et Al. "SNORD116 deletions cause all features of Prader-Willi syndrome," V. International Participated Erciyes Medical Genetics Days Congress, Nevşehir, Turkey, 2020
SEYHAN, SERHAT Et Al. "SNORD116 deletions cause all features of Prader-Willi syndrome." V. International Participated Erciyes Medical Genetics Days Congress , Nevşehir, Turkey, 2020
SEYHAN, S. Et Al. (2020) . "SNORD116 deletions cause all features of Prader-Willi syndrome." V. International Participated Erciyes Medical Genetics Days Congress , Nevşehir, Turkey.
@conferencepaper{conferencepaper, author={SERHAT SEYHAN Et Al. }, title={SNORD116 deletions cause all features of Prader-Willi syndrome}, congress name={V. International Participated Erciyes Medical Genetics Days Congress}, city={Nevşehir}, country={Turkey}, year={2020}}