Treffer 1 - 2 von 2 für Suche 'Yasun, Öztan', Suchdauer: 0,66s Treffer weiter einschränken
  1. 1
    Homozygous Mutations in Fibroblast Growth Factor 3 Are Associated with a New Form of Syndromic Deafness Characterized by Inner Ear Agenesis, Microtia, and Microdontia

    Homozygous Mutations in Fibroblast Growth Factor 3 Are Associated with a New Form of Syndromic Deafness Characterized by Inner Ear Agenesis, Microtia, and Microdontia von Tekin, Mustafa, Hişmi, Burcu Öztürk, Fitoz, Suat, Özdağ, Hilal, Cengiz, Filiz Başak, Sırmacı, Aslı, Aslan, İdil, İnceoğlu, Bora, Yüksel-Konuk, E. Berrin, Yılmaz, Seda Taşır, Yasun, Öztan, Akar, Nejat


    Volltext
    Artikel

    Zu den Favoriten
    Gespeichert in:
  2. 2
    Seckel syndrome with cutaneous pigmentary changes: two siblings and a review of the literature

    Seckel syndrome with cutaneous pigmentary changes: two siblings and a review of the literature von Kilic, Arzu, Çakmak, Seray Külcü, Tuncali, Timur, Koz, Ozlem, Ozhamamci, Esra, Yasun, Oztan, Artuz, Ferda


    Volltext
    Artikel

    Zu den Favoriten
    Gespeichert in:

Suchwerkzeuge: