The clinical and molecular features of three Turkish patients with a rare genetic disorder: 2q37 deletion syndrome.
Gürsoy S, Kutbay YB, Özdemir TR, Hazan F.
Gürsoy S, et al.
Turk J Pediatr. 2019;61(4):589-593. doi: 10.24953/turkjped.2019.04.017.
Turk J Pediatr. 2019.
PMID: 31990478
Free article.
Gursoy S, Kutbay YB, Ozdemir TR, Hazan F. The clinical and molecular features of three Turkish patients with a rare genetic disorder: 2q37 deletion syndrome. ...
Gursoy S, Kutbay YB, Ozdemir TR, Hazan F. The clinical and molecular features of three Turkish patients with a rare genetic di …