Author:
Castronovo P,Delahaye-Duriez A,Gervasini C,Azzollini J,Minier F,Russo S,Masciadri M,Selicorni A,Verloes A,Larizza L
Subject
Genetics (clinical),Genetics
Reference29 articles.
1. Cornelia de Lange syndrome: clinical review, diagnostic and scoring system, and anticipatory guidance;Kline;Am J Med Genet A,2007
2. Clinical score of 62 Italian patients with Cornelia de Lange syndrome and correlations with the presence and type of NIPBL mutation;Selicorni;Clin Genet,2007
3. Cornelia de Lange syndrome, cohesion, and beyond;Liu;Clin Genet,2009
4. Cornelia de Lange sindrome is caused by mutations in NIPBL, the human homolog of Drosophila melanogaster Nipped-B;Krantz;Nat Genet,2004
5. NIPBL, encoding a homolog of fungal Scc2-type sister chromatid cohesion proteins and fly Nipped-B, is mutated in Cornelia de Lange syndrome;Tonkin;Nat Genet,2004
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