İbrahim Vargel

Disruption of ALX1 Causes Extreme Microphthalmia and Severe Facial Clefting: Expanding the Spectrum of Autosomal-Recessive ALX-Related Frontonasal Dysplasia

Elif Uz, Yasemin Alanay, Dilek Aktaş et al. · The American Journal of Human Genetics · 2010 · 149 citations · Full text

Developmental Anomaly, Developmental Biology, Pathology +6

ALX4 dysfunction disrupts craniofacial and epidermal development

Hülya Kayserili, Elif Uz, Carien M. Niessen et al. · Human Molecular Genetics · 2009 · 120 citations · Full text

Production and characterization of hybrid nanofiber wound dressing containing Centella asiatica coated silver nanoparticles by mutual electrospinning method

Ogün Bozkaya, Esra Arat, Zehra Gün Gök et al. · European Polymer Journal · 2022 · 76 citations

Materials Science, Nanofiber, Engineering +5

Mutations in the interleukin receptor <i><scp>IL</scp>11<scp>RA</scp></i> cause autosomal recessive Crouzon‐like craniosynostosis

Katharina Keupp, Yun Li, İbrahim Vargel et al. · Molecular Genetics & Genomic Medicine · 2013 · 75 citations · Full text

Ring chromosome 4 and Wolf–Hirschhorn syndrome (WHS) in a child with multiple anomalies

Sevim Balcı, Özlem Engiz, Dilek Aktaş et al. · American Journal of Medical Genetics Part A · 2006 · 63 citations

Developmental Anomaly, Developmental Biology, Wolf-hirschhorn Syndrome +14