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Involvement of chromosome X in primary cytogenetic change in human neoplasia: nonrandom translocation in synovial sarcoma

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TLDR
The X;18 rearrangement appears to characterize the synovial sarcoma and is the first description of a primary, nonrandom change in the sex chromosome of a human solid tumor.
Abstract
A translocation that involves chromosome X (band p112) and chromosome 18 (band q112) was observed in short-term in vitro cultures of cells from five synovial sarcomas and one malignant fibrous histiocytoma In four of these tumors, the translocation t(X;18)(p112;q112) was reciprocal The two other tumors had complex translocations: t(X;18;21)(p112;q112;p13) and t(X;15;18)(p112;q23;q112) A translocation between chromosomes X and 18 was not detected in other histological types of soft tissue sarcoma The X;18 rearrangement appears to characterize the synovial sarcoma and is the first description of a primary, nonrandom change in the sex chromosome of a human solid tumor

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A cancer family syndrome in twenty-four kindreds.

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Identification of novel genes, SYT and SSX, involved in the t(X;18)(p11.2;q11.2) translocation found in human synovial sarcoma

TL;DR: Sequencing of cDNA clones shows that the normal SYT gene encodes a protein rich in glutamine, proline and glycine, and indicates that in synovial sarcoma rearrangement of the SYT genes results in the formation of an SYT–SSX fusion protein.
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Chromosome aberrations and cancer

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Pathology of Peripheral Nerve Sheath Tumors: Diagnostic Overview and Update on Selected Diagnostic Problems

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Ets-related protein Elk-1 is homologous to the c-fos regulatory factor p62TCF.

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