Showing 1 - 2 results of 2 for search 'Kadri Karaer', query time: 0.02s Refine Results
  1. 1
    A case of de novo microdeletion with combination of 1q21.1 and 14q32.2q32.31

    A case of de novo microdeletion with combination of 1q21.1 and 14q32.2q32.31 by Hale Onder Yilmaz, Kadri Karaer, Orkun Yilmaz

    Published 2020-12-01
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    Article
  2. 2
    A Novel Mutation of SCL26A4 gene in Turkish Family with Pendred Syndrome

    A Novel Mutation of SCL26A4 gene in Turkish Family with Pendred Syndrome by Ozgur Aldemir, Kadri Karaer, Cengiz Cevik, Haldun Dogan, Cumali Gokce

    Published 2015-06-01
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