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Alternative mechanisms associated with silencing of CDKN1C in Beckwith-Wiedemann syndrome.
J Med Genet. 2005 Aug;42(8):648-55. doi: 10.1136/jmg.2004.030593.
J Med Genet. 2005.
PMID: 16061564
Free PMC article.
Silencing of CDKN1C (p57KIP2) is associated with hypomethylation at KvDMR1 in Beckwith-Wiedemann syndrome.
Diaz-Meyer N, Day CD, Khatod K, Maher ER, Cooper W, Reik W, Junien C, Graham G, Algar E, Der Kaloustian VM, Higgins MJ.
Diaz-Meyer N, et al.
J Med Genet. 2003 Nov;40(11):797-801. doi: 10.1136/jmg.40.11.797.
J Med Genet. 2003.
PMID: 14627666
Free PMC article.
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Identification of novel gene amplifications in breast cancer and coexistence of gene amplification with an activating mutation of PIK3CA.
Kadota M, Sato M, Duncan B, Ooshima A, Yang HH, Diaz-Meyer N, Gere S, Kageyama S, Fukuoka J, Nagata T, Tsukada K, Dunn BK, Wakefield LM, Lee MP.
Kadota M, et al. Among authors: diaz meyer n.
Cancer Res. 2009 Sep 15;69(18):7357-65. doi: 10.1158/0008-5472.CAN-09-0064. Epub 2009 Aug 25.
Cancer Res. 2009.
PMID: 19706770
Free PMC article.
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