Uz, E. Et Al. 2010. Disruption of ALX1 Causes Extreme Microphthalmia and Severe Facial Clefting: Expanding the Spectrum of Autosomal-Recessive ALX-Related Frontonasal Dysplasia. AMERICAN JOURNAL OF HUMAN GENETICS , vol.86, no.5 , 789-796.

Uz, E., ALANAY, Y., Aktas, D., Vargel, I., Gucer, S., Tuncbilek, G., ... von Eggeling, F.(2010). Disruption of ALX1 Causes Extreme Microphthalmia and Severe Facial Clefting: Expanding the Spectrum of Autosomal-Recessive ALX-Related Frontonasal Dysplasia. AMERICAN JOURNAL OF HUMAN GENETICS , vol.86, no.5, 789-796.

Uz, Elif Et Al. "Disruption of ALX1 Causes Extreme Microphthalmia and Severe Facial Clefting: Expanding the Spectrum of Autosomal-Recessive ALX-Related Frontonasal Dysplasia," AMERICAN JOURNAL OF HUMAN GENETICS , vol.86, no.5, 789-796, 2010

Uz, Elif Et Al. "Disruption of ALX1 Causes Extreme Microphthalmia and Severe Facial Clefting: Expanding the Spectrum of Autosomal-Recessive ALX-Related Frontonasal Dysplasia." AMERICAN JOURNAL OF HUMAN GENETICS , vol.86, no.5, pp.789-796, 2010

Uz, E. Et Al. (2010) . "Disruption of ALX1 Causes Extreme Microphthalmia and Severe Facial Clefting: Expanding the Spectrum of Autosomal-Recessive ALX-Related Frontonasal Dysplasia." AMERICAN JOURNAL OF HUMAN GENETICS , vol.86, no.5, pp.789-796.

@article{article, author={Elif Uz Et Al. }, title={Disruption of ALX1 Causes Extreme Microphthalmia and Severe Facial Clefting: Expanding the Spectrum of Autosomal-Recessive ALX-Related Frontonasal Dysplasia}, journal={AMERICAN JOURNAL OF HUMAN GENETICS}, year=2010, pages={789-796} }