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Delineation of the frequency and boundary of chromosomal copy number variations in paediatric neuroblastoma
Neuroblastoma, the most common solid tumour in early childhood, is characterized by very frequent chromosomal copy number variations (CNVs). While chromosome 2p amplification, 17q gain, 1p and 11q deletion in human neuroblastoma tissues are well-known, the exact frequencies and boundaries of the chr...
Tallennettuna:
| Julkaisussa: | Cell Cycle |
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| Päätekijät: | , , , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Taylor & Francis
2018
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5969554/ https://ncbi.nlm.nih.gov/pubmed/29353549 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/15384101.2017.1421875 |
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