खोज परिणाम - Onur Emre Onat

  • प्रदर्शित 1 - 8 परिणाम 8
परिणाम को परिष्कृत करें
  1. 1
    Mutations in the very low-density lipoprotein receptor <i>VLDLR</i> cause cerebellar hypoplasia and quadrupedal locomotion in humans

    Mutations in the very low-density lipoprotein receptor <i>VLDLR</i> cause cerebellar hypoplasia and quadrupedal locomotion in humans द्वारा Tayfun Özçelık, Nurten Akarsu, Elif Uz, Şafak Çağlayan, Süleyman Gülsüner, Onur Emre Onat, Meli̇ha Tan, Üner Tan

    प्रकाशित 2008
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
    Artigo
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    में बचाया:
  2. 2
    Early postzygotic mutations contribute to de novo variation in a healthy monozygotic twin pair

    Early postzygotic mutations contribute to de novo variation in a healthy monozygotic twin pair द्वारा Gülşah M Dal, Bekir Ergüner, Mahmut Şamil Sağıroğlu, Bayram Yüksel, Onur Emre Onat, Can Alkan, Tayfun Özçelık

    प्रकाशित 2014
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    Artigo
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  3. 3
    Mutation of the Human Circadian Clock Gene CRY1 in Familial Delayed Sleep Phase Disorder

    Mutation of the Human Circadian Clock Gene CRY1 in Familial Delayed Sleep Phase Disorder द्वारा Alina Patke, Patricia Murphy, Onur Emre Onat, Ana C. Krieger, Tayfun Özçelık, Scott S. Campbell, Michael W. Young

    प्रकाशित 2017
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    Artigo
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  4. 4
    Missense mutation in the ATPase, aminophospholipid transporter protein ATP8A2 is associated with cerebellar atrophy and quadrupedal locomotion

    Missense mutation in the ATPase, aminophospholipid transporter protein ATP8A2 is associated with cerebellar atrophy and quadrupedal locomotion द्वारा Onur Emre Onat, Süleyman Gülsüner, Kaya Bilgüvar, A. Nazlı Başak, Haluk Topaloğlu, Meli̇ha Tan, Üner Tan, Murat Günel, Tayfun Özçelık

    प्रकाशित 2012
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    Artigo
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    में बचाया:
  5. 5
    Homozygosity mapping and targeted genomic sequencing reveal the gene responsible for cerebellar hypoplasia and quadrupedal locomotion in a consanguineous kindred

    Homozygosity mapping and targeted genomic sequencing reveal the gene responsible for cerebellar hypoplasia and quadrupedal locomotion in a consanguineous kindred द्वारा Süleyman Gülsüner, Ayşe B. Tekinay, Katja Doerschner, Hüseyin Boyacı, Kaya Bilgüvar, Hilal Ünal, Aslihan Ors, Onur Emre Onat, Ergin Atalar, A. Nazlı Başak, Haluk Topaloğlu, Tülay Kansu, Meli̇ha Tan, Üner Tan, Murat Günel, Tayfun Özçelık

    प्रकाशित 2011
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    Artigo
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    में बचाया:
  6. 6
    Mitochondrial serine protease HTRA2 p.G399S in a kindred with essential tremor and Parkinson disease

    Mitochondrial serine protease HTRA2 p.G399S in a kindred with essential tremor and Parkinson disease द्वारा Hilal Ünal Gülsüner, Süleyman Gülsüner, Fatma Nazlı Mercan, Onur Emre Onat, Tom Walsh, Hashem Shahin, Ming K. Lee, Okan Doğu, Tülay Kansu, Haluk Topaloğlu, Bülent Elibol, Cenk Akbostancı, Mary‐Claire King, Tayfun Özçelık, Ayşe B. Tekinay

    प्रकाशित 2014
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    Artigo
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  7. 7
    The genetic structure of the Turkish population reveals high levels of variation and admixture

    The genetic structure of the Turkish population reveals high levels of variation and admixture द्वारा Meltem Ece Kars, A. Nazlı Başak, Onur Emre Onat, Kaya Bilgüvar, Jungmin Choi, Yuval Itan, Caner Çağlar, Robin Palvadeau, Jean‐Laurent Casanova, D.N. Cooper, Peter D. Stenson, Alper Yavuz, Hakan Buluş, Murat Günel, Jeffrey M. Friedman, Tayfun Özçelık

    प्रकाशित 2021
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    Artigo
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  8. 8
    Human CRY1 variants associate with attention deficit/hyperactivity disorder

    Human CRY1 variants associate with attention deficit/hyperactivity disorder द्वारा Onur Emre Onat, Meltem Ece Kars, Şeref Gül, Kaya Bilgüvar, Yiming Wu, Ayşe Özhan, Cihan Aydın, A. Nazlı Başak, Maria Allegra Trusso, Arianna Goracci, Chiara Fallerini, Alessandra Renieri, Jean‐Laurent Casanova, Yuval Itan, Cem Atbaşoğlu, Meram Can Saka, İbrahim Halil Kavaklı, Tayfun Özçelık

    प्रकाशित 2020
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    Artigo
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