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Arunachal, G. et al. (n.d.). A novel de-novo frameshift mutation of the ASXL1 gene in a classic case of Bohring–Opitz syndrome. Clinical dysmorphology. 25 (3), p. . [Online].
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Arunachal, G. et al. (n.d.). A novel de-novo frameshift mutation of the ASXL1 gene in a classic case of Bohring–Opitz syndrome. Clinical dysmorphology. 25 (3), p. . [Online].