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Biallelic inactivation of NF1 in a sporadic plexiform neurofibroma.
Beert E, Brems H, Renard M, Ferreiro JF, Melotte C, Thoelen R, De Wever I, Sciot R, Legius E, Debiec-Rychter M. Beert E, et al. Among authors: brems h. Genes Chromosomes Cancer. 2012 Sep;51(9):852-7. doi: 10.1002/gcc.21969. Epub 2012 May 14. Genes Chromosomes Cancer. 2012. PMID: 22585738
NF2 gene deletion in a family with a mild phenotype.
López-Correa C, Zucman-Rossi J, Brems H, Thomas G, Legius E. López-Correa C, et al. Among authors: brems h. J Med Genet. 2000 Jan;37(1):75-7. doi: 10.1136/jmg.37.1.75. J Med Genet. 2000. PMID: 10691417 Free PMC article. No abstract available.
Unequal meiotic crossover: a frequent cause of NF1 microdeletions.
López Correa C, Brems H, Lázaro C, Marynen P, Legius E. López Correa C, et al. Among authors: brems h. Am J Hum Genet. 2000 Jun;66(6):1969-74. doi: 10.1086/302920. Epub 2000 Apr 20. Am J Hum Genet. 2000. PMID: 10775528 Free PMC article.
Recombination hotspot in NF1 microdeletion patients.
López-Correa C, Dorschner M, Brems H, Lázaro C, Clementi M, Upadhyaya M, Dooijes D, Moog U, Kehrer-Sawatzki H, Rutkowski JL, Fryns JP, Marynen P, Stephens K, Legius E. López-Correa C, et al. Among authors: brems h. Hum Mol Genet. 2001 Jun 15;10(13):1387-92. doi: 10.1093/hmg/10.13.1387. Hum Mol Genet. 2001. PMID: 11440991
Elevated risk for MPNST in NF1 microdeletion patients.
De Raedt T, Brems H, Wolkenstein P, Vidaud D, Pilotti S, Perrone F, Mautner V, Frahm S, Sciot R, Legius E. De Raedt T, et al. Among authors: brems h. Am J Hum Genet. 2003 May;72(5):1288-92. doi: 10.1086/374821. Epub 2003 Mar 26. Am J Hum Genet. 2003. PMID: 12660952 Free PMC article.
92 results