A region of consistent deletion in neuroblastoma maps within human chromosome 1p36.2-36.3.

Deletion of the short arm of human chromosome 1 is the most common cytogenetic abnormality observed in neuroblastoma. To characterize the region of consistent deletion, we performed loss of heterozygosity (LOH) studies on 122 neuroblastoma tumor samples with 30 distal chromosome 1p polymorphisms. LO...

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Hlavní autoři: White, P S, Maris, J M, Beltinger, C, Sulman, E, Marshall, H N, Fujimori, M, Kaufman, B A, Biegel, J A, Allen, C, Hilliard, C
Médium: Artigo
Jazyk:Inglês
Vydáno: 1995
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Research Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC41727/
https://ncbi.nlm.nih.gov/pubmed/7777541
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