Brems H - Search Results

1

Copy number variations in the NF1 gene region are infrequent and do not predispose to recurrent type-1 deletions.

Steinmann K, Kluwe L, Cooper DN, Brems H, De Raedt T, Legius E, Mautner VF, Kehrer-Sawatzki H. Steinmann K, et al. Among authors: brems h. Eur J Hum Genet. 2008 May;16(5):572-80. doi: 10.1038/sj.ejhg.5202002. Epub 2008 Jan 23. Eur J Hum Genet. 2008. PMID: 18212816

2

Molecular studies in 20 submicroscopic neurofibromatosis type 1 gene deletions.

Lopez Correa C, Brems H, Lázaro C, Estivill X, Clementi M, Mason S, Rutkowski JL, Marynen P, Legius E. Lopez Correa C, et al. Among authors: brems h. Hum Mutat. 1999;14(5):387-93. doi: 10.1002/(SICI)1098-1004(199911)14:5<387::AID-HUMU4>3.0.CO;2-4. Hum Mutat. 1999. PMID: 10533064

3

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.

4

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.

5

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

6

Hemifacial microsomia in two patients further supporting chromosomal mosaicism as a causative factor.

de Ravel TJ, Legius E, Brems H, Van Hoestenberghe R, Gillis PH, Fryns JP. de Ravel TJ, et al. Among authors: brems h. Clin Dysmorphol. 2001 Oct;10(4):263-7. doi: 10.1097/00019605-200110000-00005. Clin Dysmorphol. 2001. PMID: 11666000

7

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.

8

Second polar body inclusion results in diploid/triploid mixoploidy.

Brems H, Vogels A, Ribai P, De Raedt T, Fryns JP, Legius E. Brems H, et al. Genet Couns. 2003;14(4):425-9. Genet Couns. 2003. PMID: 14738117

9

Genetic and phenotypic characterization of tumor cells derived from malignant peripheral nerve sheath tumors of neurofibromatosis type 1 patients.

Frahm S, Mautner VF, Brems H, Legius E, Debiec-Rychter M, Friedrich RE, Knöfel WT, Peiper M, Kluwe L. Frahm S, et al. Among authors: brems h. Neurobiol Dis. 2004 Jun;16(1):85-91. doi: 10.1016/j.nbd.2004.01.006. Neurobiol Dis. 2004. PMID: 15207265

10

Genomic organization and evolution of the NF1 microdeletion region.

De Raedt T, Brems H, Lopez-Correa C, Vermeesch JR, Marynen P, Legius E. De Raedt T, et al. Among authors: brems h. Genomics. 2004 Aug;84(2):346-60. doi: 10.1016/j.ygeno.2004.03.006. Genomics. 2004. PMID: 15233998

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