1. Mahajan S, Kaur A, Singh J. Ring chromosome 22: a review of the literature and first report from India. Balkan J Med Genet. 2012;15(1):55–9.
2. Denayer E, Brems H, de Cock P, Evans GD, Van Calenbergh F, Bowers N, et al. Pathogenesis of vestibular schwannoma in ring chromosome 22. BMC Med Genet. 2009;10:97.
3. Trofatter JA, MacCollin MM, Rutter JL, Murrell JR, Duyao MP, Parry DM, et al. A novel moesin-, ezrin-, radixin-like gene is a candidate for the neurofibromatosis 2 tumor suppressor. Cell. 1993;72(5):791.
4. Agrawal H, Mery CM, Sexson Tejtel SK, Fraser CD, McKenzie ED, Qureshi AM, et al. Familial clustering of cardiac conditions in patients with anomalous aortic origin of a coronary artery and myocardial bridges. Cardiol Young. 2018;28(9):1099–105.
5. Zirn B, Arning L, Bartels I, Shoukier M, Hoffjan S, Neubauer B, et al. Ring chromosome 22 and neurofibromatosis type II: proof of two-hit model for the loss of the NF2 gene in the development of meningioma. Clin Genet. 2012;81(1):82–7.