| 1 | ALX4, FND2
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| Novel homozygous ALX4 mutation causing frontonasal dysplasia-2 in a patient with meningoencephalocele.
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| Meloni VA, Moysés-Oliveira M, Melo MC, Caneloi TP, Dantas AG, Soares MF, Fock R, Rodrigues de Nicola PD, Dias-da-Silva MR, Melaragno MI.
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| Clin Genet. Dec;88(6):593-6. doi: 10.1111/cge.12595. Epub 2015 May 11. 2015
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| 2 | ALX4, FND2
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| ALX4 gain-of-function mutations in nonsyndromic craniosynostosis.
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| 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.
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| Hum Mutat. Dec;33(12):1626-9. doi: 10.1002/humu.22166. Epub 2012 Aug 13. 2012
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| 3 | ALX4, FND2
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| ALX4 dysfunction disrupts craniofacial and epidermal development.
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| 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.
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| Hum Mol Genet 18(22):4357-66. Epub 2009 Aug 19. 2009
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