SYNE1 related cerebellar ataxia presents with variable phenotypes in a consanguineous family from Turkey von Yucesan, E., Ugur Iseri, Sibel A., Bilgic, B., Gormez, Z., Bakir Gungor, B., Sarac, A., Ozdemir, O., Sagiroglu, M., Gurvit, H., Hanagasi, H., Ozbek, U.

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DEFINING NOVEL THERAPEUTIC TARGETS FOR BPS/ IC USING A BIOINFORMATICS APPROACH von Inal Gultekin, G, Görmez, Z, Mangir, N

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Myophosphorylase (PYGM) mutations in Turkish patients with McArdle disease: A next generation sequencing study von Inal Gültekin, G, Toptaş Hekimoğlu, B, Görmez, Z, Durmuş, H, Demirci, H, Sağıroğlu, M, Parman, Y, Deymeer, F, Yılmaz, H, Pençe, S, Kurt, C, Tan, E, Özdamar, S, Giger, U, Öztürk, O, Serdaroğlu-Oflazer, P

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Statistical bias and variance of gene selection and cross validation methods: A case study on hypertension prediction von Gormez, Z., Kursun, O., Sertbas, A., Aydin, N., Seker, H.

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A concatenative Turkish text-to-speech system and evaluation process von Orhan, Z., Gormez, Z.

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G.P.114 - Myophosphorylase (PYGM) mutations in Turkish patients with McArdle disease: A next generation sequencing study von Inal Gültekin, G., Toptaş Hekimoğlu, B., Görmez, Z., Durmuş, H., Demirci, H., Sağıroğlu, M., Parman, Y., Deymeer, F., Yılmaz, H., Pençe, S., Kurt, C., Tan, E., Özdamar, S., Giger, U., Öztürk, O., Serdaroğlu-Oflazer, P.

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Evaluation of the Concatenative Turkish Text-to-Speech System von Orhan, Z., Gormez, Z.

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