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HARVARD Citation
Lehalle, D. et al. (2017). STAG1 mutations cause a novel cohesinopathy characterised by unspecific syndromic intellectual disability. Journal of medical genetics. 54 (7), pp. 479-488. [Online].
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Lehalle, D. et al. (2017). STAG1 mutations cause a novel cohesinopathy characterised by unspecific syndromic intellectual disability. Journal of medical genetics. 54 (7), pp. 479-488. [Online].