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Q41347455-40D1CCFD-733E-48E1-A2B4-FC2320D22536
Q41347455-40D1CCFD-733E-48E1-A2B4-FC2320D22536
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Statement
http://www.wikidata.org/entity/statement/Q41347455-40D1CCFD-733E-48E1-A2B4-FC2320D22536
Human T-cell tumours containing chromosome 14 inversion or translocation with breakpoints proximal to immunoglobulin joining regions at 14q32.
P2860
Q41347455-40D1CCFD-733E-48E1-A2B4-FC2320D22536
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41347455-40D1CCFD-733E-48E1-A2B4-FC2320D22536
rank
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wasDerivedFrom
dc26cb9a5ec696d666dc5b2e9c5bc59be94a29e4
P2860
A chromosome 14 inversion in a T-cell lymphoma is caused by site-specific recombination between immunoglobulin and T-cell receptor loci.