Showing 1 - 4 results of 4 for search 'Dilek Aktaş', query time: 0.01s Refine Results
  1. 1
    Analysis of MTHFR 1298A>C in addition to MTHFR 677C>T polymorphism as a risk factor for neural tube defects in the Turkish population

    Analysis of MTHFR 1298A>C in addition to MTHFR 677C>T polymorphism as a risk factor for neural tube defects in the Turkish population by Koray Boduroğlu, Yasemin Alanay, Mehmet Alikaşifoğlu, Dilek Aktaş, Ergül Tunçbilek

    Published 2005-10-01
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  2. 2
    Pseudo-trisomy 13 in a fetus: further support for autosomal recessive inheritance

    Pseudo-trisomy 13 in a fetus: further support for autosomal recessive inheritance by G Eda Utine, Yasemin Alanay, Dilek Aktaş, Beril Talim, Gülsev Kale, Ergül Tunçbilek

    Published 2008-06-01
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  3. 3
    Jervell and Lange-Nielsen syndrome with homozygous missense mutation of the KCNQ1 gene

    Jervell and Lange-Nielsen syndrome with homozygous missense mutation of the KCNQ1 gene by Esra Kılıç, İlker Ertuğrul, Sema Özer, Mehmet Alikaşifoğlu, Dilek Aktaş, Koray Boduroğlu, Gülen Eda Ütine

    Published 2014-10-01
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  4. 4
    Subtelomeric rearrangements in mental retardation: Hacettepe University experience in 130 patients

    Subtelomeric rearrangements in mental retardation: Hacettepe University experience in 130 patients by Gülen Eda Utine, Tolga Celik, Yasemin Alanay, Mehmet Alikaşifoğlu, Koray Boduroğlu, Ergül Tunçbilek, Dilek Aktaş

    Published 2009-06-01
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