PubMed (OMIM) for id: 60529

Year	Number of Results
1995	1
1996	1
1997	1
1998	2
2000	2
2001	1
2006	1
2007	1
2008	1
2009	1
2011	1
2012	2
2013	1
2014	2
2024	0

1

Mild nasal clefting may be predictive for ALX4 heterozygotes.

Altunoglu U, Satkın B, Uyguner ZO, Kayserili H. Altunoglu U, et al. Am J Med Genet A. 2014 Aug;164A(8):2054-8. doi: 10.1002/ajmg.a.36578. Epub 2014 Apr 24. Am J Med Genet A. 2014. PMID: 24764194

2

Skull defects, alopecia, hypertelorism, and notched alae nasi caused by homozygous ALX4 gene mutation.

Kariminejad A, Bozorgmehr B, Alizadeh H, Ghaderi-Sohi S, Toksoy G, Uyguner ZO, Kayserili H. Kariminejad A, et al. Am J Med Genet A. 2014 May;164A(5):1322-7. doi: 10.1002/ajmg.a.36008. Epub 2014 Mar 25. Am J Med Genet A. 2014. PMID: 24668755 No abstract available.

3

Vertical transmission of a frontonasal phenotype caused by a novel ALX4 mutation.

Bertola DR, Rodrigues MG, Quaio CR, Kim CA, Passos-Bueno MR. Bertola DR, et al. Am J Med Genet A. 2013 Mar;161A(3):600-4. doi: 10.1002/ajmg.a.35762. Epub 2013 Feb 7. Am J Med Genet A. 2013. PMID: 23401352

4

ALX4 gain-of-function mutations in nonsyndromic craniosynostosis.

Yagnik G, Ghuman A, Kim S, Stevens CG, Kimonis V, Stoler J, Sanchez-Lara PA, Bernstein JA, Naydenov C, Drissi H, Cunningham ML, Kim J, Boyadjiev SA. Yagnik G, et al. Hum Mutat. 2012 Dec;33(12):1626-9. doi: 10.1002/humu.22166. Epub 2012 Aug 13. Hum Mutat. 2012. PMID: 22829454 Free PMC article.

5

Mild nasal malformations and parietal foramina caused by homozygous ALX4 mutations.

Kayserili H, Altunoglu U, Ozgur H, Basaran S, Uyguner ZO. Kayserili H, et al. Am J Med Genet A. 2012 Jan;158A(1):236-44. doi: 10.1002/ajmg.a.34390. Epub 2011 Dec 2. Am J Med Genet A. 2012. PMID: 22140057

6

ALX4 dysfunction disrupts craniofacial and epidermal development.

Kayserili H, Uz E, Niessen C, Vargel I, Alanay Y, Tuncbilek G, Yigit G, Uyguner O, Candan S, Okur H, Kaygin S, Balci S, Mavili E, Alikasifoglu M, Haase I, Wollnik B, Akarsu NA. Kayserili H, et al. Hum Mol Genet. 2009 Nov 15;18(22):4357-66. doi: 10.1093/hmg/ddp391. Epub 2009 Aug 19. Hum Mol Genet. 2009. PMID: 19692347

7

Skull defects, alopecia and distinctive facies: a new syndrome?

Kariminejad A, Bozorgmehr B, Ashrafi MR, Kariminejad MH. Kariminejad A, et al. Clin Dysmorphol. 2008 Jul;17(3):203-205. doi: 10.1097/MCD.0b013e3282fba59d. Clin Dysmorphol. 2008. PMID: 18541970 No abstract available.

8

Genetic analysis of non-syndromic craniosynostosis.

Boyadjiev SA; International Craniosynostosis Consortium. Boyadjiev SA, et al. Orthod Craniofac Res. 2007 Aug;10(3):129-37. doi: 10.1111/j.1601-6343.2007.00393.x. Orthod Craniofac Res. 2007. PMID: 17651129 Review.

9

Enlarged parietal foramina caused by mutations in the homeobox genes ALX4 and MSX2: from genotype to phenotype.

Mavrogiannis LA, Taylor IB, Davies SJ, Ramos FJ, Olivares JL, Wilkie AO. Mavrogiannis LA, et al. Eur J Hum Genet. 2006 Feb;14(2):151-8. doi: 10.1038/sj.ejhg.5201526. Eur J Hum Genet. 2006. PMID: 16319823 Free PMC article.

10

Haploinsufficiency of the human homeobox gene ALX4 causes skull ossification defects.

Mavrogiannis LA, Antonopoulou I, Baxová A, Kutílek S, Kim CA, Sugayama SM, Salamanca A, Wall SA, Morriss-Kay GM, Wilkie AO. Mavrogiannis LA, et al. Nat Genet. 2001 Jan;27(1):17-8. doi: 10.1038/83703. Nat Genet. 2001. PMID: 11137991

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