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A 22-year French experience with solid tumors in children with Down syndrome.
Satgé D, Sasco AJ, Chompret A, Orbach D, Méchinaud F, Lacour B, Roullet B, Martelli H, Bergeron C, Bertrand Y, Lacombe D, Perel Y, Monteil P, Nelken B, Bertozzi AI, Munzer M, Kanold J, Bernard F, Vekemans MJ, Sommelet D. Satgé D, et al. Among authors: vekemans mj. Pediatr Hematol Oncol. 2003 Oct-Nov;20(7):517-29. doi: 10.1080/08880010390232727. Pediatr Hematol Oncol. 2003. PMID: 12959856
A very rare cancer in Down syndrome: medulloblastoma. Epidemiological data from 13 countries.
Satgé D, Stiller CA, Rutkowski S, von Bueren AO, Lacour B, Sommelet D, Nishi M, Massimino M, Garré ML, Moreno F, Hasle H, Jakab Z, Greenberg M, von der Weid N, Kuehni C, Zurriaga O, Vicente ML, Peris-Bonet R, Benesch M, Vekemans M, Sullivan SG, Rickert C. Satgé D, et al. J Neurooncol. 2013 Mar;112(1):107-14. doi: 10.1007/s11060-012-1041-y. Epub 2013 Jan 11. J Neurooncol. 2013. PMID: 23307327 Free article.
A tumor profile in Edwards syndrome (trisomy 18).
Satgé D, Nishi M, Sirvent N, Vekemans M. Satgé D, et al. Am J Med Genet C Semin Med Genet. 2016 Sep;172(3):296-306. doi: 10.1002/ajmg.c.31511. Epub 2016 Jul 30. Am J Med Genet C Semin Med Genet. 2016. PMID: 27474103 Review.
A tumor profile in Patau syndrome (trisomy 13).
Satgé D, Nishi M, Sirvent N, Vekemans M, Chenard MP, Barnes A. Satgé D, et al. Am J Med Genet A. 2017 Aug;173(8):2088-2096. doi: 10.1002/ajmg.a.38294. Epub 2017 May 25. Am J Med Genet A. 2017. PMID: 28544599 Review.
Array-based comparative genomic hybridization identifies a high frequency of copy number variations in patients with syndromic overgrowth.
Malan V, Chevallier S, Soler G, Coubes C, Lacombe D, Pasquier L, Soulier J, Morichon-Delvallez N, Turleau C, Munnich A, Romana S, Vekemans M, Cormier-Daire V, Colleaux L. Malan V, et al. Eur J Hum Genet. 2010 Feb;18(2):227-32. doi: 10.1038/ejhg.2009.162. Epub 2009 Oct 21. Eur J Hum Genet. 2010. PMID: 19844265 Free PMC article.
299 results