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6. Deletion 1p in a low-grade chondrosarcoma in a patient with Ollier disease. Ozisik YY; Meloni AM; Spanier SS; Bush CH; Kingsley KL; Sandberg AA Cancer Genet Cytogenet; 1998 Sep; 105(2):128-33. PubMed ID: 9723029 [TBL] [Abstract][Full Text] [Related]
7. Combined array-comparative genomic hybridization and single-nucleotide polymorphism-loss of heterozygosity analysis reveals complex genetic alterations in cervical cancer. Kloth JN; Oosting J; van Wezel T; Szuhai K; Knijnenburg J; Gorter A; Kenter GG; Fleuren GJ; Jordanova ES BMC Genomics; 2007 Feb; 8():53. PubMed ID: 17311676 [TBL] [Abstract][Full Text] [Related]
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12. Loss-of-function mutations in PTPN11 cause metachondromatosis, but not Ollier disease or Maffucci syndrome. Bowen ME; Boyden ED; Holm IA; Campos-Xavier B; Bonafé L; Superti-Furga A; Ikegawa S; Cormier-Daire V; Bovée JV; Pansuriya TC; de Sousa SB; Savarirayan R; Andreucci E; Vikkula M; Garavelli L; Pottinger C; Ogino T; Sakai A; Regazzoni BM; Wuyts W; Sangiorgi L; Pedrini E; Zhu M; Kozakewich HP; Kasser JR; Seidman JG; Kurek KC; Warman ML PLoS Genet; 2011 Apr; 7(4):e1002050. PubMed ID: 21533187 [TBL] [Abstract][Full Text] [Related]
13. Enchondromatosis: insights on the different subtypes. Pansuriya TC; Kroon HM; Bovée JV Int J Clin Exp Pathol; 2010 Jun; 3(6):557-69. PubMed ID: 20661403 [TBL] [Abstract][Full Text] [Related]
14. Somatic mosaic IDH1 and IDH2 mutations are associated with enchondroma and spindle cell hemangioma in Ollier disease and Maffucci syndrome. Pansuriya TC; van Eijk R; d'Adamo P; van Ruler MA; Kuijjer ML; Oosting J; Cleton-Jansen AM; van Oosterwijk JG; Verbeke SL; Meijer D; van Wezel T; Nord KH; Sangiorgi L; Toker B; Liegl-Atzwanger B; San-Julian M; Sciot R; Limaye N; Kindblom LG; Daugaard S; Godfraind C; Boon LM; Vikkula M; Kurek KC; Szuhai K; French PJ; Bovée JV Nat Genet; 2011 Nov; 43(12):1256-61. PubMed ID: 22057234 [TBL] [Abstract][Full Text] [Related]
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17. PTHR1 mutations associated with Ollier disease result in receptor loss of function. Couvineau A; Wouters V; Bertrand G; Rouyer C; Gérard B; Boon LM; Grandchamp B; Vikkula M; Silve C Hum Mol Genet; 2008 Sep; 17(18):2766-75. PubMed ID: 18559376 [TBL] [Abstract][Full Text] [Related]
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19. Common somatic alterations identified in maffucci syndrome by molecular karyotyping. Amyere M; Dompmartin A; Wouters V; Enjolras O; Kaitila I; Docquier PL; Godfraind C; Mulliken JB; Boon LM; Vikkula M Mol Syndromol; 2014 Dec; 5(6):259-67. PubMed ID: 25565925 [TBL] [Abstract][Full Text] [Related]
20. Loss of heterozygosity and DNA ploidy point to a diverging genetic mechanism in the origin of peripheral and central chondrosarcoma. Bovée JV; Cleton-Jansen AM; Kuipers-Dijkshoorn NJ; van den Broek LJ; Taminiau AH; Cornelisse CJ; Hogendoorn PC Genes Chromosomes Cancer; 1999 Nov; 26(3):237-46. PubMed ID: 10502322 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]