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HARVARD Citation
Stavropoulos, D. et al. (n.d.). MG-130 Utilising whole exome sequencing to identify causative variants in genetically heterogeneous disorders. Journal of medical genetics. p. A11. [Online].
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Stavropoulos, D. et al. (n.d.). MG-130 Utilising whole exome sequencing to identify causative variants in genetically heterogeneous disorders. Journal of medical genetics. p. A11. [Online].