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Osteosclerotic bone dysplasia in siblings with a Fam20C mutation.
Fradin M, Stoetzel C, Muller J, Koob M, Christmann D, Debry C, Kohler M, Isnard M, Astruc D, Desprez P, Zorres C, Flori E, Dollfus H, Doray B. Fradin M, et al. Among authors: koob m. Clin Genet. 2011 Aug;80(2):177-83. doi: 10.1111/j.1399-0004.2010.01516.x. Epub 2010 Jul 23. Clin Genet. 2011. PMID: 20825432
Raine syndrome: expanding the radiological spectrum.
Koob M, Doray B, Fradin M, Astruc D, Dietemann JL. Koob M, et al. Pediatr Radiol. 2011 Mar;41(3):389-93. doi: 10.1007/s00247-010-1875-4. Epub 2010 Nov 13. Pediatr Radiol. 2011. PMID: 21076826
Cerebral tumors: specific features in children.
Koob M, Girard N. Koob M, et al. Diagn Interv Imaging. 2014 Oct;95(10):965-83. doi: 10.1016/j.diii.2014.06.017. Epub 2014 Aug 20. Diagn Interv Imaging. 2014. PMID: 25150727 Free article. Review.
[Magnetic resonance imaging of the brain].
Koob M, Dietemann JL. Koob M, et al. Presse Med. 2007 Mar;36(3 Pt 2):492-5. doi: 10.1016/j.lpm.2006.11.004. Epub 2006 Dec 13. Presse Med. 2007. PMID: 17336858 French.
117 results