Cite
HARVARD Citation
Bronstein, R. et al. (2020). A combined RNA-seq and whole genome sequencing approach for identification of non-coding pathogenic variants in single families. Human molecular genetics. pp. 967-979. [Online].
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Bronstein, R. et al. (2020). A combined RNA-seq and whole genome sequencing approach for identification of non-coding pathogenic variants in single families. Human molecular genetics. pp. 967-979. [Online].