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Page 1
Characteristics of small breast and/or ovarian cancer families with germline mutations in BRCA1 and BRCA2.
Ligtenberg MJ, Hogervorst FB, Willems HW, Arts PJ, Brink G, Hageman S, Bosgoed EA, Van der Looij E, Rookus MA, Devilee P, Vos EM, Wigbout G, Struycken PM, Menko FH, Rutgers EJ, Hoefsloot EH, Mariman EC, Brunner HG, Van 't Veer LJ. Ligtenberg MJ, et al. Among authors: van der looij e. Br J Cancer. 1999 Mar;79(9-10):1475-8. doi: 10.1038/sj.bjc.6690235. Br J Cancer. 1999. PMID: 10188893 Free PMC article.
A familial case of renal cell carcinoma and a t(2;3) chromosome translocation.
Koolen MI, van der Meyden AP, Bodmer D, Eleveld M, van der Looij E, Brunner H, Smits A, van den Berg E, Smeets D, Geurts van Kessel A. Koolen MI, et al. Among authors: van der looij e. Kidney Int. 1998 Feb;53(2):273-5. doi: 10.1046/j.1523-1755.1998.00762.x. Kidney Int. 1998. PMID: 9461085 Free article.
Germline epigenetic silencing of the tumor suppressor gene PTPRJ in early-onset familial colorectal cancer.
Venkatachalam R, Ligtenberg MJ, Hoogerbrugge N, Schackert HK, Görgens H, Hahn MM, Kamping EJ, Vreede L, Hoenselaar E, van der Looij E, Goossens M, Churchman M, Carvajal-Carmona L, Tomlinson IP, de Bruijn DR, Van Kessel AG, Kuiper RP. Venkatachalam R, et al. Among authors: van der looij e. Gastroenterology. 2010 Dec;139(6):2221-4. doi: 10.1053/j.gastro.2010.08.063. Epub 2010 Oct 29. Gastroenterology. 2010. PMID: 21036128 No abstract available.
A hereditary spastic paraplegia predominant phenotype caused by variants in the NEFL gene.
Mul K, Schouten MI, van der Looij E, Dooijes D, Hennekam FAM, Notermans NC, Praamstra P, van Gaalen J, Kamsteeg EJ, Verbeek NE, van de Warrenburg BPC. Mul K, et al. Among authors: van der looij e. Parkinsonism Relat Disord. 2020 Nov;80:98-101. doi: 10.1016/j.parkreldis.2020.09.016. Epub 2020 Sep 12. Parkinsonism Relat Disord. 2020. PMID: 32979786 Free article.