𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Genome-wide analysis of genetic alterations in Barrett's adenocarcinoma using single nucleotide polymorphism arrays

✍ Scribed by Nikolopoulos, Elisabeth; Weis, Roland; Langer, Rupert; Bartholomé, Kilian; Timmer, Jens; Wiech, Thorsten; Walch, Axel K; Höfler, Heinz; Werner, Martin

Book ID
109885258
Publisher
Nature Publishing Group
Year
2008
Tongue
English
Weight
357 KB
Volume
89
Category
Article
ISSN
0023-6837

No coin nor oath required. For personal study only.

📜 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 📂 Article 📅 2009 🏛 John Wiley and Sons 🌐 French ⚖ 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

Characterization of chromosome arm 20q a
Characterization of chromosome arm 20q abnormalities in myeloid malignancies using genome-wide single nucleotide polymorphism array analysis
✍ Jungwon Huh; Ramon V. Tiu; Lukasz P. Gondek; Christine L. O'Keefe; Monika Jasek; 📂 Article 📅 2010 🏛 John Wiley and Sons 🌐 English ⚖ 189 KB

## Abstract Deletion of the long arm of chromosome 20 is a common abnormality associated with myeloid malignancies. We characterized abnormalities of chromosome 20 as defined by metaphase cytogenetics (MC) in patients with myeloid neoplasms to define commonly deleted regions (CDR) and commonly reta

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; 📂 Article 📅 2011 🏛 John Wiley and Sons 🌐 English ⚖ 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__