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Liu, J. et al. (2021). A novel Xp11.22–22.33 deletion suggesting a possible mechanism of congenital cervical spinal muscular atrophy. Molecular genetics & genomic medicine. 9 (3), p. n/a. [Online].
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Liu, J. et al. (2021). A novel Xp11.22–22.33 deletion suggesting a possible mechanism of congenital cervical spinal muscular atrophy. Molecular genetics & genomic medicine. 9 (3), p. n/a. [Online].