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HARVARD Citation
Taylan, F. et al. (n.d.). Spondyloocular Syndrome: Novel Mutations in XYLT2 Gene and Expansion of the Phenotypic Spectrum. Journal of bone and mineral research. pp. 1577-1585. [Online].
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Taylan, F. et al. (n.d.). Spondyloocular Syndrome: Novel Mutations in XYLT2 Gene and Expansion of the Phenotypic Spectrum. Journal of bone and mineral research. pp. 1577-1585. [Online].