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 , 789-96.

Uz, E., Alanay, Y., Aktas, D., Vargel, I., Gucer, S., Tuncbilek, G., ... von, E.(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, 789-96.

Uz, ELİF 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, 789-96, 2010

Uz, ELİF U. 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, pp.789-96, 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, pp.789-96.

@article{article, author={ELİF UZ YILDIRIM 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={789-96} }