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HARVARD Citation
Alazami, A. et al. (n.d.). Novel IFT122 mutation associated with impaired ciliogenesis and cranioectodermal dysplasia. Molecular genetics & genomic medicine. 2 (2), pp. 103-106. [Online].
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Alazami, A. et al. (n.d.). Novel IFT122 mutation associated with impaired ciliogenesis and cranioectodermal dysplasia. Molecular genetics & genomic medicine. 2 (2), pp. 103-106. [Online].