Published in Hum Genet on December 01, 1997
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Fusion of the EWS and CHOP genes in myxoid liposarcoma. Oncogene (1996) 1.77
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Multiple unrelated clonal chromosome abnormalities in an in situ squamous cell carcinoma of the skin. Cancer Genet Cytogenet (1988) 1.48
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Hydroxyapatite coating of threaded pins enhances fixation. J Bone Joint Surg Br (1997) 1.41
Trisomy 7 in short-term cultures of colorectal adenocarcinomas. Genes Chromosomes Cancer (1991) 1.41
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New chromosomal rearrangement, t(12;22)(p13;q12), in acute nonlymphocytic leukemia. Cancer Genet Cytogenet (1991) 1.39
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Chromosome aberrations in 35 primary ovarian carcinomas. Genes Chromosomes Cancer (1992) 1.34
Cytogenetic deletion maps of hematologic neoplasms: circumstantial evidence for tumor suppressor loci. Genes Chromosomes Cancer (1993) 1.32
The structure and dynamics of ring chromosomes in human neoplastic and non-neoplastic cells. Hum Genet (1999) 1.31
Genetic convergence and divergence in tumor progression. Cancer Res (1988) 1.31
Cytogenetic analysis of subcutaneous angiolipoma: further evidence supporting its difference from ordinary pure lipomas: a report of the CHAMP Study Group. Am J Surg Pathol (1997) 1.30
Clodronate prevents prosthetic migration: a randomized radiostereometric study of 50 total knee patients. Acta Orthop Scand (2000) 1.29
Germline MSH2 and MLH1 mutational spectrum including large rearrangements in HNPCC families from Poland (update study). Clin Genet (2006) 1.29
Lipomas have characteristic structural chromosomal rearrangements of 12q13-q14. Int J Cancer (1987) 1.28
Chromosomal abnormalities involving 11q13 are associated with poor prognosis in patients with squamous cell carcinoma of the head and neck. Cancer (1995) 1.28
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Translocation X;18 in synovial sarcoma. Cancer Genet Cytogenet (1986) 1.26
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Nonrandom chromosomal rearrangements in pancreatic carcinomas. Cancer (1992) 1.19
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Cytogenetic characterization of peripheral nerve sheath tumours: a report of the CHAMP study group. J Pathol (2000) 1.18
In situ hybridization localizes the human putative oncogene GLI to chromosome subbands 12q13.3-14.1. Hum Genet (1989) 1.18
Chromosomal organization of amplified chromosome 12 sequences in mesenchymal tumors detected by fluorescence in situ hybridization. Genes Chromosomes Cancer (1998) 1.18
Cytogenetic-morphologic correlations in aneurysmal bone cyst, giant cell tumor of bone and combined lesions. A report from the CHAMP study group. Mod Pathol (2000) 1.18
Hibernomas are characterized by rearrangements of chromosome bands 11q13-21. Int J Cancer (1994) 1.17
Oncogenic conversion of a novel orphan nuclear receptor by chromosome translocation. Hum Mol Genet (1995) 1.17
The SYT-SSX1 variant of synovial sarcoma is associated with a high rate of tumor cell proliferation and poor clinical outcome. Cancer Res (1999) 1.16
Characterization of the CHOP breakpoints and fusion transcripts in myxoid liposarcomas with the 12;16 translocation. Cancer Res (1994) 1.16
Magnetic resonance imaging, scintigraphy, and arthroscopic evaluation of traumatic hemarthrosis of the knee. Am J Sports Med (1997) 1.16
Open-wedge osteotomy by hemicallotasis or the closed-wedge technique for osteoarthritis of the knee. A randomised study of 50 operations. J Bone Joint Surg Br (1999) 1.16
Analysis of 35 cases of localized and diffuse tenosynovial giant cell tumor: a report from the Chromosomes and Morphology (CHAMP) study group. Mod Pathol (1999) 1.15
POU5F1, encoding a key regulator of stem cell pluripotency, is fused to EWSR1 in hidradenoma of the skin and mucoepidermoid carcinoma of the salivary glands. J Pathol (2008) 1.15
Monosomy and trisomy of 15q24----qter in a family with a translocation t(6;15)(p25;q24). Clin Genet (1987) 1.15
Chromosome analysis of 97 primary breast carcinomas: identification of eight karyotypic subgroups. Genes Chromosomes Cancer (1995) 1.15
Additional evidence of a variant translocation t(12;22) with EWS/CHOP fusion in myxoid liposarcoma: clinicopathological features. J Pathol (1997) 1.15