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Four novel SCN1A mutations in Turkish patients with severe myoclonic epilepsy of infancy (SMEI). [electronic resource] by
- Arlier, Zulfikar
- Bayri, Yasar
- Kolb, Luis E
- Erturk, Ozdem
- Ozturk, Ali K
- Bayrakli, Fatih
- Bilguvar, Kaya
- Moliterno, Jennifer A
- Dervent, Aysin
- Demirbilek, Veysi
- Yalcinkaya, Cengiz
- Korkmaz, Baris
- Tuysuz, Beyhan
- Gunel, Murat
Producer: 20110815
In:
Journal of child neurology vol. 25
Availability: No items available.
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Novel VLDLR microdeletion identified in two Turkish siblings with pachygyria and pontocerebellar atrophy. [electronic resource] by
- Kolb, Luis E
- Arlier, Zulfikar
- Yalcinkaya, Cengiz
- Ozturk, Ali K
- Moliterno, Jennifer A
- Erturk, Ozdem
- Bayrakli, Fatih
- Korkmaz, Baris
- DiLuna, Michael L
- Yasuno, Katsuhito
- Bilguvar, Kaya
- Ozcelik, Tayfun
- Tuysuz, Beyhan
- State, Matthew W
- Gunel, Murat
Producer: 20100924
In:
Neurogenetics vol. 11
Availability: No items available.
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Genomic analysis of non-NF2 meningiomas reveals mutations in TRAF7, KLF4, AKT1, and SMO. [electronic resource] by
- Clark, Victoria E
- Erson-Omay, E Zeynep
- Serin, Akdes
- Yin, Jun
- Cotney, Justin
- Ozduman, Koray
- Avşar, Timuçin
- Li, Jie
- Murray, Phillip B
- Henegariu, Octavian
- Yilmaz, Saliha
- Günel, Jennifer Moliterno
- Carrión-Grant, Geneive
- Yilmaz, Baran
- Grady, Conor
- Tanrikulu, Bahattin
- Bakircioğlu, Mehmet
- Kaymakçalan, Hande
- Caglayan, Ahmet Okay
- Sencar, Leman
- Ceyhun, Emre
- Atik, A Fatih
- Bayri, Yaşar
- Bai, Hanwen
- Kolb, Luis E
- Hebert, Ryan M
- Omay, S Bulent
- Mishra-Gorur, Ketu
- Choi, Murim
- Overton, John D
- Holland, Eric C
- Mane, Shrikant
- State, Matthew W
- Bilgüvar, Kaya
- Baehring, Joachim M
- Gutin, Philip H
- Piepmeier, Joseph M
- Vortmeyer, Alexander
- Brennan, Cameron W
- Pamir, M Necmettin
- Kiliç, Türker
- Lifton, Richard P
- Noonan, James P
- Yasuno, Katsuhito
- Günel, Murat
Producer: 20130307
In:
Science (New York, N.Y.) vol. 339
Availability: No items available.
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