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HARVARD Citation
Makrythanasis, P. et al. (2016). Exome sequencing discloses KALRN homozygous variant as likely cause of intellectual disability and short stature in a consanguineous pedigree. Human genomics. 10 (1), pp. 1-7. [Online].
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Makrythanasis, P. et al. (2016). Exome sequencing discloses KALRN homozygous variant as likely cause of intellectual disability and short stature in a consanguineous pedigree. Human genomics. 10 (1), pp. 1-7. [Online].