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 Aktas, Ibrahim Vargel, Safak Gucer, Gokhan Tuncbilek, Ferdinand von Eggeling, Engin Yilmaz, Ozgur Deren, Nicole Posorski, Hilal Ozdag, Thomas Liehr, Sevim Balci, Mehmet Alikasifoglu, Bernd Wollnik, Nurten A. Akarsu
  • The American Journal of Human Genetics, May 2010, Elsevier
  • DOI: 10.1016/j.ajhg.2010.04.002
The author haven't finished explaining this publicationThe author haven't finished explaining this publication
The following have contributed to this page: Professor Ferdinand von Eggeling