Legius E - Search Results

1

Phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha (PIK3CA)-related overgrowth spectrum: A brief report.

Denorme P, Morren MA, Hollants S, Spaepen M, Suaer K, Zutterman N, Labarque V, Legius E, Brems H. Denorme P, et al. Among authors: legius e. Pediatr Dermatol. 2018 May;35(3):e186-e188. doi: 10.1111/pde.13441. Epub 2018 Mar 1. Pediatr Dermatol. 2018. PMID: 29493003

2

Increased and decreased relative risk for non-insulin-dependent diabetes mellitus conferred by HLA class II and by CD4 alleles.

Ghabanbasani MZ, Spaepen M, Buyse I, Legius E, Decorte R, Bex M, Marynen P, Bouillon R, Cassiman JJ. Ghabanbasani MZ, et al. Among authors: legius e. Clin Genet. 1995 May;47(5):225-30. doi: 10.1111/j.1399-0004.1995.tb04301.x. Clin Genet. 1995. PMID: 7554346

3

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: legius e. 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

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: legius e. 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: legius e. 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: legius e. 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: legius e. 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. Among authors: legius e. Genet Couns. 2003;14(4):425-9. Genet Couns. 2003. PMID: 14738117

9

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: legius e. Genomics. 2004 Aug;84(2):346-60. doi: 10.1016/j.ygeno.2004.03.006. Genomics. 2004. PMID: 15233998

10

Germline mutations of the hMLH1 and hMSH2 mismatch repair genes in Belgian hereditary nonpolyposis colon cancer (HNPCC) patients.

Spaepen M, Vankeirsbilck B, Van Opstal S, Tejpar S, Van Cutsem E, Geboes K, Legius E, Matthijs G. Spaepen M, et al. Among authors: legius e. Fam Cancer. 2006;5(2):179-89. doi: 10.1007/s10689-005-5958-6. Fam Cancer. 2006. PMID: 16736289

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