Frontonasal dysplasia
Definition:
References:
-
[1]. Elif Uz, et al. Disruption of ALX1 causes extreme microphthalmia and severe facial clefting: expanding the spectrum of autosomal-recessive ALX-related frontonasal dysplasia. Am J Hum Genet. 2010 May 14;86(5):789-96. [Content Brief]
[2]. Hulya Kayserili, et al. ALX4 dysfunction disrupts craniofacial and epidermal development. Hum Mol Genet. 2009 Nov 15;18(22):4357-66. [Content Brief]
[3]. Karam A Allam, et al. The spectrum of median craniofacial dysplasia. Plast Reconstr Surg. 2011 Feb;127(2):812-821. [Content Brief]
[4]. Samantha A Brugmann, et al. Craniofacial ciliopathies: A new classification for craniofacial disorders. Am J Med Genet A. 2010 Dec;152A(12):2995-3006. [Content Brief]
[5]. Stephen R F Twigg, et al. Frontorhiny, a distinctive presentation of frontonasal dysplasia caused by recessive mutations in the ALX3 homeobox gene. Am J Hum Genet. 2009 May;84(5):698-705. [Content Brief]
Molarity Calculator
Dilution Calculator
