Showing 1 - 7 results of 7 for search 'Duygu Duman', query time: 0.04s Refine Results
  1. 1
    Genetic Causes of Inner Ear Anomalies: a Review from the Turkish Study Group for Inner Ear Anomalies

    Genetic Causes of Inner Ear Anomalies: a Review from the Turkish Study Group for Inner Ear Anomalies by Emre Ocak, Duygu Duman, Mustafa Tekin

    Published 2019-07-01
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  2. 2
    Whole Mitochondrial Genome Analysis in Turkish Patients With Mitochondrial Diseases

    Whole Mitochondrial Genome Analysis in Turkish Patients With Mitochondrial Diseases by Emine Begüm Gencer Öncül, Duygu Duman, Fatma Tuba Eminoğlu, Süleyman Aktuna, Mustafa Türker Duman

    Published 2022-03-01
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  3. 3
    Novel GPR156 variants confirm its role in moderate sensorineural hearing loss

    Novel GPR156 variants confirm its role in moderate sensorineural hearing loss by Memoona Ramzan, Nazim Bozan, Serhat Seyhan, Mohammad Faraz Zafeer, Aburrahman Ayral, Duygu Duman, Guney Bademci, Mustafa Tekin

    Published 2023-10-01
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  4. 4
    Identification of candidate gene FAM183A and novel pathogenic variants in known genes: High genetic heterogeneity for autosomal recessive intellectual disability.

    Identification of candidate gene FAM183A and novel pathogenic variants in known genes: High genetic heterogeneity for autosomal recessive intellectual disability. by Megan McSherry, Katherine E Masih, Nursel H Elcioglu, Pelin Celik, Ozge Balci, Filiz Basak Cengiz, Daniella Nunez, Claire J Sineni, Serhat Seyhan, Defne Kocaoglu, Shengru Guo, Duygu Duman, Guney Bademci, Mustafa Tekin

    Published 2018-01-01
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  5. 5
    Correction: Whole-Exome Sequencing Efficiently Detects Rare Mutations in Autosomal Recessive Nonsyndromic Hearing Loss.

    Correction: Whole-Exome Sequencing Efficiently Detects Rare Mutations in Autosomal Recessive Nonsyndromic Hearing Loss. by Oscar Diaz-Horta, Duygu Duman, Joseph Foster, Aslı Sırmacı, Michael Gonzalez, Nejat Mahdieh, Nikou Fotouhi, Mortaza Bonyadi, Filiz Başak Cengiz, Ibis Menendez, Rick H. Ulloa, Yvonne J. K. Edwards, Stephan Züchner, Susan Blanton, Mustafa Tekin

    Published 2013-01-01
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  6. 6
    Whole-exome sequencing efficiently detects rare mutations in autosomal recessive nonsyndromic hearing loss.

    Whole-exome sequencing efficiently detects rare mutations in autosomal recessive nonsyndromic hearing loss. by Oscar Diaz-Horta, Duygu Duman, Joseph Foster, Aslı Sırmacı, Michael Gonzalez, Nejat Mahdieh, Nikou Fotouhi, Mortaza Bonyadi, Filiz Başak Cengiz, Ibis Menendez, Rick H Ulloa, Yvonne J K Edwards, Stephan Züchner, Susan Blanton, Mustafa Tekin

    Published 2012-01-01
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  7. 7
    Dispersed DNA variants underlie hearing loss in South Florida’s minority population

    Dispersed DNA variants underlie hearing loss in South Florida’s minority population by LéShon Peart, Joanna Gonzalez, Dayna Morel Swols, Duygu Duman, Turcin Saridogan, Memoona Ramzan, Mohammad Faraz Zafeer, Xue Zhong Liu, Adrien A. Eshraghi, Michael E. Hoffer, Simon I. Angeli, Guney Bademci, Susan Blanton, Carson Smith, Fred F. Telischi, Mustafa Tekin

    Published 2023-11-01
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