𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Genome-wide DNA copy number analysis in pancreatic cancer using high-density single nucleotide polymorphism arrays

✍ Scribed by Harada, T; Chelala, C; Bhakta, V; Chaplin, T; Caulee, K; Baril, P; Young, B D; Lemoine, N R

Book ID
110072818
Publisher
Nature Publishing Group
Year
2007
Tongue
English
Weight
535 KB
Volume
27
Category
Article
ISSN
0950-9232

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

Genome-wide profiling of chromosomal alt
Genome-wide profiling of chromosomal alterations in renal cell carcinoma using high-density single nucleotide polymorphism arrays
✍ Meng Chen; Yuanqing Ye; Hushan Yang; Pheroze Tamboli; Surena Matin; Nizar M. Tan πŸ“‚ Article πŸ“… 2009 πŸ› John Wiley and Sons 🌐 French βš– 198 KB

## Abstract The identification of genetic aberrations may help understand the mechanisms of tumorigenesis and has important implications in diagnosis, prognosis and treatment. We applied Illumina's 317K high‐density single nucleotide polymorphism (SNP) arrays to profile chromosomal aberrations in c

Maffucci syndrome: A genome-wide analysi
Maffucci syndrome: A genome-wide analysis using high resolution single nucleotide polymorphism and expression arrays on four cases
✍ Twinkal C. Pansuriya; Jan Oosting; Suzan H. M. Verdegaal; Adrienne M. Flanagan; πŸ“‚ Article πŸ“… 2011 πŸ› John Wiley and Sons 🌐 English βš– 892 KB

## Abstract Ollier disease and Maffucci syndrome are rare, nonhereditary skeletal disorders characterized by the presence of multiple enchondromas with (Maffucci) or without (Ollier) co‐existing multiple hemangiomas of soft tissue. Enchondromas can progress toward central chondrosarcomas. __PTH1R__