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HARVARD Citation
Pacault, M. et al. (2018). New splicing pathogenic variant in EBP causing extreme familial variability of Conradi–Hünermann–Happle Syndrome. European journal of human genetics. pp. 1784-1790. [Online].
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Pacault, M. et al. (2018). New splicing pathogenic variant in EBP causing extreme familial variability of Conradi–Hünermann–Happle Syndrome. European journal of human genetics. pp. 1784-1790. [Online].