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Human T-cell tumours containing chromosome 14 inversion or translocation with breakpoints proximal to immunoglobulin joining regions at 14q32.

T-cell tumours are frequently found to carry an inversion of chromosome 14 (inv(14)) (q11;q32) or more rarely a chromosome 14 translocation t(14;14) with the same cytogenetic breakpoints (q11;q32). We have examined the molecular junctions of an inv(14) and a translocation t(14;14) using T-cell recep...

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Autors principals: Mengle-Gaw, L, Willard, H F, Smith, C I, Hammarström, L, Fischer, P, Sherrington, P, Lucas, G, Thompson, P W, Baer, R, Rabbitts, T H
Format: Artigo
Idioma:Inglês
Publicat: 1987
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Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC553629/
https://ncbi.nlm.nih.gov/pubmed/3117531
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