Makrythanasis, P., Guipponi, M., Santoni, F. A., Zaki, M., Issa, M. Y., Ansar, M., . . . Antonarakis, S. E. (2016). Exome sequencing discloses KALRN homozygous variant as likely cause of intellectual disability and short stature in a consanguineous pedigree. Hum Genomics.

Makrythanasis, Periklis, Michel Guipponi, Federico A. Santoni, Maha Zaki, Mahmoud Y. Issa, Muhammad Ansar, Hanan Hamamy, و Stylianos E. Antonarakis. "Exome Sequencing Discloses KALRN Homozygous Variant As Likely Cause of Intellectual Disability and Short Stature in a Consanguineous Pedigree." Hum Genomics 2016.

Makrythanasis, Periklis, et al. "Exome Sequencing Discloses KALRN Homozygous Variant As Likely Cause of Intellectual Disability and Short Stature in a Consanguineous Pedigree." Hum Genomics 2016.