NIPBL mutations and genetic heterogeneity in Cornelia de Lange syndrome.
Borck G, Redon R, Sanlaville D, Rio M, Prieur M, Lyonnet S, Vekemans M, Carter NP, Munnich A, Colleaux L, Cormier-Daire V.
Borck G, et al. Among authors: redon r.
J Med Genet. 2004 Dec;41(12):e128. doi: 10.1136/jmg.2004.026666.
J Med Genet. 2004.
PMID: 15591270
Free PMC article.
No abstract available.