E. Uctepe
发表
M. Gunduz,
E. Uctepe,
E. Gunduz,
2013
.
T. Ohtsuki,
H. Wake,
T. Nishinaka,
2021,
Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie.
R. Yiğitoğlu,
E. Uctepe,
E. Gunduz,
2015
.
Golder N Wilson,
A. V. Vulto-van Silfhout,
R. Pfundt,
2018,
Genetics in Medicine.
O. Balçik,
O. Hatipoglu,
M. Gunduz,
2015,
Medicine.
Hüseyin Demirci,
M. Gunduz,
F. M. Sonmez,
2016,
Intractable & rare diseases research.
A. V. Vulto-van Silfhout,
R. Pfundt,
B. D. de Vries,
2019,
Genetics in Medicine.
M. Gunduz,
E. Uctepe,
E. Gunduz,
2014
.
E. Uctepe,
E. Gunduz,
M. Acar,
2014
.
M. Alikaşifoğlu,
F. M. Sonmez,
Fatma Mujgan Sonmez,
2017,
Intractable & rare diseases research.
Patricia H. Wheeler,
A. V. Vulto-van Silfhout,
R. Pfundt,
2018,
Genetics in Medicine.
KCNB1 frameshift variant caused inherited intellectual disability, developmental delay, and seizure.
E. Uctepe,
Sait Tümer,
Hanifenur Mancılar,
2022,
Intractable & rare diseases research.
F. M. Sonmez,
E. Uctepe,
Bekir Erguner,
2023,
Clinical dysmorphology.