Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Akgumus, Gozde Tugce"'
Autor:
Caglayan, Ahmet Okay, Baranoski, Jacob F., Aktar, Fesih, Han, Wengi, Tuysuz, Beyhan, Guzel, Aslan, Guclu, Bulent, Kaymakcalan, Hande, Aktekin, Berrin, Akgumus, Gozde Tugce, Murray, Phillip B., Erson-Omay, Emine Z., Caglar, Caner, Bakircioglu, Mehmet, Sakalar, Yildirim Bayezit, Guzel, Ebru, Demir, Nihat, Tuncer, Oguz, Senturk, Senem, Ekici, Baris, Minja, Frank J., Šestan, Nenad, Yasuno, Katsuhito, Bilguvar, Kaya, Caksen, Huseyin, Gunel, Murat
Publikováno v:
In Pediatric Neurology December 2014 51(6):806-813
Akademický článek
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Autor:
McEvoy-Venneri, Jennifer, Einhorn, Yaron, Guemez-Gamboa, Alicia, Heimer, Gali, Bilguvar, Kaya, Musaev, Damir, Shomron, Noam, Porat, Yuval, Akizu, Naiara, Gabriel, Stacey, Pillar, Nir, Issa, Mahmoud Y., Erson-Omay, Emine Z., Gregor, Anne, PER, HÜSEYİN, Ben-Zeev, Bruria, Gunel, Murat, Yasuno, Katsuhito, Fang, Rebecca, Copeland, Brett, Saleem, Sahar N., Rosti, Rasim Ozgur, Silhavy, Jennifer L., Belandres, Denice, Lewis, Steven M., Weissglas-Volkov, Daphna, Caglayan, Ahmet Okay, Akgumus, Gozde Tugce, Gumus, Hakan, Gleeson, Joseph G., Kumandas, Sefer, Stanley, Valentina, Bayram, Ayse Kacar, Schroth, Jana, Zaki, Maha S.
Objective Methods To identify causes of the autosomal-recessive malformation, diencephalic-mesencephalic junction dysplasia (DMJD) syndrome. Eight families with DMJD were studied by whole-exome or targeted sequencing, with detailed clinical and radio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::568fadac39f9538092edf10f83a7a3da
https://europepmc.org/articles/PMC6510237/
https://europepmc.org/articles/PMC6510237/
Akademický článek
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K zobrazení výsledku je třeba se přihlásit.
Autor:
Caglayan, Ahmet Okay, Aktar, Fesih, Bilguvar, Kaya, Baranoski, Jacob F., Akgumus, Gozde Tugce, Harmanci, Akdes Serin, Erson-Omay, Emine Zeynep, Yasuno, Katsuhito, Caksen, Huseyin, Gunel, Murat
Publikováno v:
Journal of Human Genetics; February 2021, Vol. 66 Issue: 2 p215-218, 4p
Autor:
Caglayan, Ahmet Okay, Comu, Sinan, Baranoski, Jacob F., Parman, Yesim, Kaymakçalan, Hande, Akgumus, Gozde Tugce, Caglar, Caner, Dolen, Duygu, Erson-Omay, Emine Zeynep, Harmanci, Akdes Serin, Mishra-Gorur, Ketu, Freeze, Hudson H., Yasuno, Katsuhito, Bilguvar, Kaya, Gunel, Murat
Publikováno v:
In European Journal of Medical Genetics January 2015 58(1):39-43
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
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Autor:
Caglayan AO; Department of Medical Genetics, School of Medicine, Dokuz Eylul University, 35340, Izmir, Turkey. ahmetokay.caglayan@deu.edu.tr., Aktar F; Department of Pediatrics, School of Medicine, Dicle University, 21060, Diyarbakir, Turkey., Bilguvar K; Department of Genetics, Yale Center for Genome Analysis, Yale School of Medicine, New Haven, CT, 06510, USA., Baranoski JF; Department of Neurosurgery, Neurobiology and Genetics, New Haven, CT, 06520-8082, USA., Akgumus GT; Department of Neurosurgery, Neurobiology and Genetics, New Haven, CT, 06520-8082, USA., Harmanci AS; Department of Neurosurgery, Neurobiology and Genetics, New Haven, CT, 06520-8082, USA., Erson-Omay EZ; Department of Neurosurgery, Neurobiology and Genetics, New Haven, CT, 06520-8082, USA., Yasuno K; Department of Neurosurgery, Neurobiology and Genetics, New Haven, CT, 06520-8082, USA., Caksen H; Division of Pediatric Neurology and Genetics, Department of Pediatrics, Meram Medical Faculty, Necmettin Erbakan University, 42080, Konya, Turkey., Gunel M; Department of Neurosurgery, Neurobiology and Genetics, New Haven, CT, 06520-8082, USA.
Publikováno v:
Journal of human genetics [J Hum Genet] 2021 Feb; Vol. 66 (2), pp. 215-218. Date of Electronic Publication: 2020 Aug 06.