Author:
Urreizti Roser,Cueto-Gonzalez Anna Maria,Franco-Valls Héctor,Mort-Farre Sílvia,Roca-Ayats Neus,Ponomarenko Julia,Cozzuto Luca,Company Carlos,Bosio Mattia,Ossowski Stephan,Montfort Magda,Hecht Jochen,Tizzano Eduardo F.,Cormand Bru,Vilageliu Lluïsa,Opitz John M.,Neri Giovanni,Grinberg Daniel,Balcells Susana
Publisher
Springer Science and Business Media LLC
Reference27 articles.
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3. Kaname, T. et al. Mutations in CD96, a member of the immunoglobulin superfamily, cause a form of the C (Opitz trigonocephaly) syndrome. Am. J. Hum. Genet. 81, 835–841 (2007).
4. Darlow, J. M., McKay, L., Dobson, M. G., Barton, D. E. & Winship, I. On the origins of renal cell carcinoma, vesicoureteric reflux and C (Opitz trigonocephaly) syndrome: A complex puzzle revealed by the sequencing of an inherited t(2;3) translocation. Eur. J. Hum. Genet. 21, 145 (2013).
5. Urreizti, R. et al. Screening of CD96 and ASXL1 in 11 patients with Opitz C or Bohring-Opitz syndromes. Am. J. Med. Genet. A 170, 24–31 (2016).
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