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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Publicado en:	EMBO J
Autores principales:	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
Formato:	Artigo
Lenguaje:	Inglês
Publicado:	Nature Publishing Group 1987
Materias:	Research Article
Acceso en línea:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC553629/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/3117531/ https://ncbi.nlm.nih.govhttps://doi.org/10.1002/j.1460-2075.1987.tb02501.x
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