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Journal of Medical Genetics|September 4, 2023
Biallelic truncating variants in <i>VGLL2</i> cause syngnathia in humansValeria Agostini, Aude Tessier, Nabila Djaziri, et al.American Journal of Human Genetics|May 11, 2010
Disruption of ALX1 causes extreme microphthalmia and severe facial clefting: expanding the spectrum of autosomal-recessive ALX-related frontonasal dysplasiaElif Uz, Yasemin Alanay, Dilek Aktas, et al.Human Molecular Genetics|August 21, 2009
ALX4 dysfunction disrupts craniofacial and epidermal developmentHulya Kayserili, Elif Uz, Carien Niessen, et al.Pageof 2