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G Haliloğlu

Showing results (1-10 of 4) with videos related to

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Molecular Syndromology|April 19, 2012
Searching for Copy Number Changes in Nonsyndromic X-Linked Intellectual DisabilityG E Utine, P Ö Kiper, Y Alanay, et al.
American Journal of Medical Genetics. Part A|November 22, 2013
Neurochemical evaluation of brain function with 1H magnetic resonance spectroscopy in patients with fragile X syndromeG E Utine, B Akpınar, U Arslan, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|June 9, 2005
Beta-sarcoglycan gene mutations in TurkeyB Balci, E Wilichowski, G Haliloğlu, et al.
Journal of Medical Genetics|June 21, 2015
Joubert syndrome: a model for untangling recessive disorders with extreme genetic heterogeneityR Bachmann-Gagescu, J C Dempsey, I G Phelps, et al.
Pageof 1

Showing results (1-10 of 4) with videos related to

Sort By:
Pageof 1
Molecular Syndromology|April 19, 2012
Searching for Copy Number Changes in Nonsyndromic X-Linked Intellectual DisabilityG E Utine, P Ö Kiper, Y Alanay, et al.
American Journal of Medical Genetics. Part A|November 22, 2013
Neurochemical evaluation of brain function with 1H magnetic resonance spectroscopy in patients with fragile X syndromeG E Utine, B Akpınar, U Arslan, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|June 9, 2005
Beta-sarcoglycan gene mutations in TurkeyB Balci, E Wilichowski, G Haliloğlu, et al.
Journal of Medical Genetics|June 21, 2015
Joubert syndrome: a model for untangling recessive disorders with extreme genetic heterogeneityR Bachmann-Gagescu, J C Dempsey, I G Phelps, et al.
Pageof 1