ATMIŞ, B. Et Al. 2021. An Orphan Dısease Mımıckıng Bartter Syndrome: Congenıtal Dısorders Of Glycosylatıon Type IIk.. 53rd ESPN Annual Meeting .

ATMIŞ, B., BULUT, F. D., KOR, D., CEVİZLİ, D., SARIBAŞ, E., ÇAĞLI, Ç., ... KARABAY BAYAZIT, A.(2021). An Orphan Dısease Mımıckıng Bartter Syndrome: Congenıtal Dısorders Of Glycosylatıon Type IIk. . 53rd ESPN Annual Meeting

ATMIŞ, BAHRİYE Et Al. "An Orphan Dısease Mımıckıng Bartter Syndrome: Congenıtal Dısorders Of Glycosylatıon Type IIk.," 53rd ESPN Annual Meeting, 2021

ATMIŞ, BAHRİYE Et Al. "An Orphan Dısease Mımıckıng Bartter Syndrome: Congenıtal Dısorders Of Glycosylatıon Type IIk.." 53rd ESPN Annual Meeting , 2021

ATMIŞ, B. Et Al. (2021) . "An Orphan Dısease Mımıckıng Bartter Syndrome: Congenıtal Dısorders Of Glycosylatıon Type IIk.." 53rd ESPN Annual Meeting .

@conferencepaper{conferencepaper, author={BAHRİYE ATMIŞ Et Al. }, title={An Orphan Dısease Mımıckıng Bartter Syndrome: Congenıtal Dısorders Of Glycosylatıon Type IIk.}, congress name={53rd ESPN Annual Meeting}, city={}, country={}, year={2021}}