Showing 1 - 4 results of 4 for search 'Filiz Hazan', query time: 0.02s Refine Results
  1. 1
    The clinical and molecular features of three Turkish patients with a rare genetic disorder: 2q37 deletion syndrome

    The clinical and molecular features of three Turkish patients with a rare genetic disorder: 2q37 deletion syndrome by Semra Gürsoy, Yaşar Bekir Kutbay, Taha Reşid Özdemir, Filiz Hazan

    Published 2019-08-01
    Get full text
    Article
    Save to List
    Saved in:
  2. 2
    A Rare Case of Cystic Hygroma and Familial Nystagmus in a Newborn with SHOC2 Gene Mutation

    A Rare Case of Cystic Hygroma and Familial Nystagmus in a Newborn with SHOC2 Gene Mutation by Suzan Süncak, Filiz Hazan, Coşkun Armağan, Ceren Yılmaz Uzman, Semra Gürsoy, Özlem Giray Bozkaya

    Published 2025-08-01
    Get full text
    Article
    Save to List
    Saved in:
  3. 3
    Child with RET proto-oncogene codon 634 mutation

    Child with RET proto-oncogene codon 634 mutation by Dilek İnce, Kamer Mutafoglu, Erdener Özer, Ayhan Abacı, Filiz Hazan, Osman Zeki Karakuş, Hale Tuhan, Yeşim Oymak, Eda Ataseven, Bengü Demirağ, Nur Olgun

    Published 2017-10-01
    Get full text
    Article
    Save to List
    Saved in:
  4. 4
    Sequence and copy number analyses of HEXB gene in patients affected by Sandhoff disease: functional characterization of 9 novel sequence variants.

    Sequence and copy number analyses of HEXB gene in patients affected by Sandhoff disease: functional characterization of 9 novel sequence variants. by Stefania Zampieri, Silvia Cattarossi, Ana Maria Oller Ramirez, Camillo Rosano, Charles Marques Lourenco, Nadia Passon, Isabella Moroni, Graziella Uziel, Antonella Pettinari, Franco Stanzial, Raquel Dodelson de Kremer, Nydia Beatriz Azar, Filiz Hazan, Mirella Filocamo, Bruno Bembi, Andrea Dardis

    Published 2012-01-01
    Get full text
    Article
    Save to List
    Saved in:

Search Tools: