Ş. ALTINER Et Al. , "Clinical findings in 22q11.2 microdeletion syndrome: case series," EUROPEAN JOURNAL OF HUMAN GENETICS , vol.30, no.SUPPL 1, pp.325, 2022
ALTINER, Ş. Et Al. 2022. Clinical findings in 22q11.2 microdeletion syndrome: case series. EUROPEAN JOURNAL OF HUMAN GENETICS , vol.30, no.SUPPL 1 , 325.
ALTINER, Ş., TUNCALI, T., KUTLAY, N., KARABULUT, H. G., & ILGIN RUHİ, H., (2022). Clinical findings in 22q11.2 microdeletion syndrome: case series. EUROPEAN JOURNAL OF HUMAN GENETICS , vol.30, no.SUPPL 1, 325.
ALTINER, ŞULE Et Al. "Clinical findings in 22q11.2 microdeletion syndrome: case series," EUROPEAN JOURNAL OF HUMAN GENETICS , vol.30, no.SUPPL 1, 325, 2022
ALTINER, ŞULE Et Al. "Clinical findings in 22q11.2 microdeletion syndrome: case series." EUROPEAN JOURNAL OF HUMAN GENETICS , vol.30, no.SUPPL 1, pp.325, 2022
ALTINER, Ş. Et Al. (2022) . "Clinical findings in 22q11.2 microdeletion syndrome: case series." EUROPEAN JOURNAL OF HUMAN GENETICS , vol.30, no.SUPPL 1, p.325.
@article{article, author={ŞULE ALTINER Et Al. }, title={Clinical findings in 22q11.2 microdeletion syndrome: case series}, journal={EUROPEAN JOURNAL OF HUMAN GENETICS}, year=2022, pages={325} }