Characterization of renal cell carcinoma‐associated constitutional chromosome abnormalities by genome sequencing

Constitutional translocations, typically involving chromosome 3, have been recognized as a rare cause of inherited predisposition to renal cell carcinoma (RCC) for four decades. However, knowledge of the molecular basis of this association is limited. We have characterized the breakpoints by genome...

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Detalles Bibliográficos
Autores principales: Smith, Philip S., Whitworth, James, West, Hannah, Cook, Jacqueline, Gardiner, Carol, Lim, Derek H. K., Morrison, Patrick J., Hislop, R. Gordon, Murray, Emily, Tischkowitz, Marc, Warren, Anne Y., Woodward, Emma R., Maher, Eamonn R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2020
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7187337/
https://www.ncbi.nlm.nih.gov/pubmed/31943436
http://dx.doi.org/10.1002/gcc.22833

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7187337/
https://www.ncbi.nlm.nih.gov/pubmed/31943436
http://dx.doi.org/10.1002/gcc.22833

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