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Germline APC mutation spectrum derived from 863 genomic variations identified through a 15-year medical genetics service to French patients with FAP.
Lagarde A, Rouleau E, Ferrari A, Noguchi T, Qiu J, Briaux A, Bourdon V, Rémy V, Gaildrat P, Adélaïde J, Birnbaum D, Lidereau R, Sobol H, Olschwang S. Lagarde A, et al. Among authors: remy v. J Med Genet. 2010 Oct;47(10):721-2. doi: 10.1136/jmg.2010.078964. Epub 2010 Aug 3. J Med Genet. 2010. PMID: 20685668 Free article.
Y253H mutation appearing in a micro-BCR-ABL (e19a2) CML.
Popovici C, Charbonnier A, Gisserot O, Aguilon P, Rémy V, Olschwang S, Mozziconacci MJ. Popovici C, et al. Among authors: remy v. Leuk Res. 2008 Feb;32(2):361-2. doi: 10.1016/j.leukres.2007.03.001. Epub 2007 Apr 6. Leuk Res. 2008. PMID: 17412419 No abstract available.
t(5;12)(q23-31;p13) with ETV6-ACSL6 gene fusion in polycythemia vera.
Murati A, Adélaïde J, Gelsi-Boyer V, Etienne A, Rémy V, Fezoui H, Sainty D, Xerri L, Vey N, Olschwang S, Birnbaum D, Chaffanet M, Mozziconacci MJ. Murati A, et al. Among authors: remy v. Leukemia. 2006 Jun;20(6):1175-8. doi: 10.1038/sj.leu.2404194. Leukemia. 2006. PMID: 16572202 No abstract available.
70 results