Four novel NIPBL mutations in Japanese patients with Cornelia de Lange syndrome.
Miyake N, Visser R, Kinoshita A, Yoshiura K, Niikawa N, Kondoh T, Matsumoto N, Harada N, Okamoto N, Sonoda T, Naritomi K, Kaname T, Chinen Y, Tonoki H, Kurosawa K.
Miyake N, et al. Among authors: kaname t.
Am J Med Genet A. 2005 May 15;135(1):103-5. doi: 10.1002/ajmg.a.30637.
Am J Med Genet A. 2005.
PMID: 15723327
Free article.
No abstract available.