Cited by

• A new mutation of the PCNT gene in a Colombian patient with microcephalic osteodysplastic primordial dwarfism type II: a case report.

  Pachajoa H, Ruiz-Botero F, Isaza C. Pachajoa H, et al. J Med Case Rep. 2014 Jun 13;8:191. doi: 10.1186/1752-1947-8-191. J Med Case Rep. 2014. PMID: 24928221 Free PMC article.
• Mechanisms and pathways of growth failure in primordial dwarfism.

  Klingseisen A, Jackson AP. Klingseisen A, et al. Genes Dev. 2011 Oct 1;25(19):2011-24. doi: 10.1101/gad.169037. Genes Dev. 2011. PMID: 21979914 Free PMC article. Review.
• The Effects of ATIR Blocker on the Severity of COVID-19 in Hypertensive Inpatients and Virulence of SARS-CoV-2 in Hypertensive hACE2 Transgenic Mice.

  Jiang X, Li H, Liu Y, Bao L, Zhan L, Gao H, Deng W, Xue J, Liu J, Liu X, Li J, Wang J, Wu S, Yan M, Luo W, Jose PA, Qin C, Yang X, Zhang D, Yang Z. Jiang X, et al. J Cardiovasc Transl Res. 2022 Feb;15(1):38-48. doi: 10.1007/s12265-021-10147-3. Epub 2022 Jan 1. J Cardiovasc Transl Res. 2022. PMID: 34973134 Free PMC article.
• Analysis of centrosome and DNA damage response in PLK4 associated Seckel syndrome.

  Dinçer T, Yorgancıoğlu-Budak G, Ölmez A, Er İ, Dodurga Y, Özdemir ÖM, Toraman B, Yıldırım A, Sabir N, Akarsu NA, Semerci CN, Kalay E. Dinçer T, et al. Eur J Hum Genet. 2017 Oct;25(10):1118-1125. doi: 10.1038/ejhg.2017.120. Epub 2017 Aug 23. Eur J Hum Genet. 2017. PMID: 28832566 Free PMC article.
• Biallelic variants in DNA2 cause microcephalic primordial dwarfism.

  Tarnauskaitė Ž, Bicknell LS, Marsh JA, Murray JE, Parry DA, Logan CV, Bober MB, de Silva DC, Duker AL, Sillence D, Wise C, Jackson AP, Murina O, Reijns MAM. Tarnauskaitė Ž, et al. Hum Mutat. 2019 Aug;40(8):1063-1070. doi: 10.1002/humu.23776. Epub 2019 Jun 23. Hum Mutat. 2019. PMID: 31045292 Free PMC article.