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

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 Volume 86, Issue 5, Pages 789-796 (May 2010)

DOI: 10.1016/j.ajhg.2010.04.002

Copyright © 2010 The American Society of Human Genetics Terms and Conditions

http://www.elsevier.com/termsandconditions

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The American Journal of Human Genetics 2010 86, 789-796DOI: (10.1016/j.ajhg.2010.04.002) Copyright © 2010 The American Society of Human Genetics Terms and Conditions


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

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