Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

MyNCBI Filters
Text availability
Article attribute
Article type
Publication date

Search Results

385 results
Filters applied: . Clear all Results are displayed in a computed author sort order. Results by year timeline is unavailable
Page 1
Gain of chromosome arm 17q and adverse outcome in patients with neuroblastoma.
Bown N, Cotterill S, Lastowska M, O'Neill S, Pearson AD, Plantaz D, Meddeb M, Danglot G, Brinkschmidt C, Christiansen H, Laureys G, Speleman F, Nicholson J, Bernheim A, Betts DR, Vandesompele J, Van Roy N. Bown N, et al. Among authors: Speleman F. N Engl J Med. 1999 Jun 24;340(25):1954-61. doi: 10.1056/NEJM199906243402504. N Engl J Med. 1999. PMID: 10379019 Clinical Trial.
Molecular cytogenetic definition of 17q translocation breakpoints in neuroblastoma.
Lastowska M, Van Roy N, Bown N, Speleman F, Roberts P, Lunec J, Strachan T, Pearson AD, Jackson MS. Lastowska M, et al. Among authors: Speleman F. Med Pediatr Oncol. 2001 Jan;36(1):20-3. doi: 10.1002/1096-911X(20010101)36:1<20::AID-MPO1006>3.0.CO;2-E. Med Pediatr Oncol. 2001. PMID: 11464884 Clinical Trial.
Molecular cytogenetic delineation of 17q translocation breakpoints in neuroblastoma cell lines.
Lastowska M, Van Roy N, Bown N, Speleman F, Lunec J, Strachan T, Pearson AD, Jackson MS. Lastowska M, et al. Among authors: Speleman F. Genes Chromosomes Cancer. 1998 Oct;23(2):116-22. doi: 10.1002/(sici)1098-2264(199810)23:2<116::aid-gcc4>3.0.co;2-5. Genes Chromosomes Cancer. 1998. PMID: 9739014
Balanced translocation in a neuroblastoma patient disrupts a cluster of small nuclear RNA U1 and tRNA genes in chromosomal band 1p36.
van der Drift P, Chan A, Laureys G, van Roy N, Sickmann G, den Dunnen J, Westerveld A, Speleman F, Versteeg R. van der Drift P, et al. Among authors: Speleman F. Genes Chromosomes Cancer. 1995 Sep;14(1):35-42. doi: 10.1002/gcc.2870140107. Genes Chromosomes Cancer. 1995. PMID: 8527382
Chromosome aberrations in fibrous dysplasia.
Dal Cin P, Sciot R, Speleman F, Samson I, Laureys G, de Potter C, Meire F, van Damme B, van den Berghe H. Dal Cin P, et al. Among authors: Speleman F. Cancer Genet Cytogenet. 1994 Oct 15;77(2):114-7. doi: 10.1016/0165-4608(94)90225-9. Cancer Genet Cytogenet. 1994. PMID: 7954320
Further delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a severe outcome.
van Bon BW, Mefford HC, Menten B, Koolen DA, Sharp AJ, Nillesen WM, Innis JW, de Ravel TJ, Mercer CL, Fichera M, Stewart H, Connell LE, Ounap K, Lachlan K, Castle B, Van der Aa N, van Ravenswaaij C, Nobrega MA, Serra-Juhé C, Simonic I, de Leeuw N, Pfundt R, Bongers EM, Baker C, Finnemore P, Huang S, Maloney VK, Crolla JA, van Kalmthout M, Elia M, Vandeweyer G, Fryns JP, Janssens S, Foulds N, Reitano S, Smith K, Parkel S, Loeys B, Woods CG, Oostra A, Speleman F, Pereira AC, Kurg A, Willatt L, Knight SJ, Vermeesch JR, Romano C, Barber JC, Mortier G, Pérez-Jurado LA, Kooy F, Brunner HG, Eichler EE, Kleefstra T, de Vries BB. van Bon BW, et al. Among authors: Speleman F. J Med Genet. 2009 Aug;46(8):511-23. doi: 10.1136/jmg.2008.063412. Epub 2009 Apr 15. J Med Genet. 2009. PMID: 19372089 Free PMC article.
385 results
Jump to page
Feedback