Cite
HARVARD Citation
Khateb, S. et al. (2016). Identification of genomic deletions causing inherited retinal degenerations by coverage analysis of whole exome sequencing data. Journal of medical genetics. 53 (9), pp. 600-607. [Online].
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Khateb, S. et al. (2016). Identification of genomic deletions causing inherited retinal degenerations by coverage analysis of whole exome sequencing data. Journal of medical genetics. 53 (9), pp. 600-607. [Online].