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Author/Creator Ergüner, Bekir

2. Finding underlying genetic mechanisms of two patients with autism spectrum disorder carrying familial apparently balanced chromosomal translocations. (11th March 2021)

Authors:
Toraman, Bayram; Bilginer, Samiye Çilem; Hesapçıoğlu, Selma Tural; Göker, Zeynep; Soykam, Hüseyin Okan; Ergüner, Bekir; Dinçer, Tuba; Yıldız, Gökhan; Ünsal, Serbülent; Kasap, Burak Kaan; Kandil, Sema; Kalay, Ersan
Journal:
Journal of gene medicine
Issue:
Volume 23:Number 4(2021)
Page Start:
n/a
Record Type:
Journal Article
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3. The DNA methylation landscape of glioblastoma disease progression shows extensive heterogeneity in time and space. (October 2018)

Authors:
Klughammer, Johanna; Kiesel, Barbara; Roetzer, Thomas; Fortelny, Nikolaus; Nemc, Amelie; Nenning, Karl-Heinz; Furtner, Julia; Sheffield, Nathan; Datlinger, Paul; Peter, Nadine; Nowosielski, Martha; Augustin, Marco; Mischkulnig, Mario; Ströbel, Thomas; Alpar, Donat; Ergüner, Bekir; Senekowitsch, M...
Journal:
Nature medicine
Issue:
Volume 24:Number 10(2018)
Page Start:
1611
Record Type:
Journal Article
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4. TMCO1 deficiency causes autosomal recessive cerebrofaciothoracic dysplasia. Issue 2 (5th November 2013)

Authors:
Alanay, Yasemin; Ergüner, Bekir; Utine, Eda; Haçarız, Orçun; Kiper, Pelin Ozlem Simsek; Taşkıran, Ekim Zihni; Perçin, Ferda; Uz, Elif; Sağıroğlu, Mahmut Şamil; Yuksel, Bayram; Boduroglu, Koray; Akarsu, Nurten Ayse
Journal:
American journal of medical genetics
Issue:
Volume 164:Issue 2(2014.)
Page Start:
291
Record Type:
Journal Article
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