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...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: 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
Formato: Artigo
Lenguaje:Inglês
Publicado: 1995
Materias:
Research Article
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC41727/
https://ncbi.nlm.nih.gov/pubmed/7777541
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!

Ejemplares similares