ALX1

Publications

Dee C et al. Defective neural crest migration revealed by a Zebrafish model of Alx1-related frontonasal dysplasia. Hum Mol Genet. 2013;22(2):239-51.  PMID: 23059813.

Kayserili H et al. ALX4 dysfunction disrupts craniofacial and epidermal development. Hum Mol Genet. 2009;18(22):4357-66.  PMID: 19692347.

Meijlink F et al. Vertebrate aristaless-related genes. Int J Dev Biol. 1999;43(7):651-63.  PMID: 10668975.

Twigg SR et al. Frontorhiny, a distinctive presentation of frontonasal dysplasia caused by recessive mutations in the ALX3 homeobox gene. Am J Hum Genet. 2009;84(5):698-705.  PMID: 19409524.

Ullah A et al. Exome sequencing revealed a novel splice site variant in the ALX1 gene underlying frontonasal dysplasia. Clin Genet. 2017;91(3):494-498.  PMID: 27324866.

Uz E 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;86(5):789-96.  PMID: 20451171.

Zhao Q et al. Prenatal folic acid treatment suppresses acrania and meroanencephaly in mice mutant for the Cart1 homeobox gene. Nat Genet. 1996;13(3):275-83.  PMID: 8673125.