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©The Author(s) 2020.
World J Med Genet. Jun 20, 2020; 9(1): 1-11
Published online Jun 20, 2020. doi: 10.5496/wjmg.v9.i1.1
Published online Jun 20, 2020. doi: 10.5496/wjmg.v9.i1.1
Figure 1 A patient with Wiedemann-Steiner syndrome.
Her peculiar facial features include marked vertical narrowing of the palpebral fissures, hypertelorism, arched eyebrows, epicanthus, wide nasal bridge, low-set ears, and long philtrum.
- Citation: Fontana P, Passaretti FF, Maioli M, Cantalupo G, Scarano F, Lonardo F. Clinical and molecular spectrum of Wiedemann-Steiner syndrome, an emerging member of the chromatinopathy family. World J Med Genet 2020; 9(1): 1-11
- URL: https://www.wjgnet.com/2220-3184/full/v9/i1/1.htm
- DOI: https://dx.doi.org/10.5496/wjmg.v9.i1.1