𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Low Frequency of Chromosomal Imbalances in Anaplastic Ependymomas as Detected by Comparative Genomic Hybridization

✍ Scribed by Stefanie Scheil; Silke Brüderlein; Monika Eicker; Jochen Herms; Christel Herold-Mende; Hans-Herbert Steiner; Thomas F. E. Barth; Peter Möller

Book ID
111404113
Publisher
John Wiley and Sons
Year
2006
Tongue
English
Weight
245 KB
Volume
11
Category
Article
ISSN
1015-6305

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Chromosomal imbalances detected by array
Chromosomal imbalances detected by array comparative genomic hybridization in human oligodendrogliomas and mixed oligoastrocytomas
✍ Gaspar Kitange; Anjan Misra; Mark Law; Sandra Passe; Thomas M. Kollmeyer; Matthe 📂 Article 📅 2004 🏛 John Wiley and Sons 🌐 English ⚖ 619 KB

## Abstract Loss of heterozygosity and fluorescence in situ hybridization (FISH) studies have shown that deletions of 1p and 19q are highly prevalent in oligodendroglioma. However, these tumors have not been comprehensively screened for other alterations in chromosomal dosage. In this study, we use

Low frequency of numerical chromosomal a
Low frequency of numerical chromosomal aberrations in follicular thyroid tumors detected by comparative genomic hybridization
✍ Tony Frisk; Soili Kytölä; Göran Wallin; Jan Zedenius; Catharina Larsson 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 110 KB 👁 1 views

Follicular thyroid tumors vary from adenomas to widely invasive carcinomas, and a stepwise progression from normal thyrocyte to malignant tumor has been suggested to be due to an accumulation of genetic alterations. We have used comparative genomic hybridization to screen 21 follicular thyroid tumor

Chromosome imbalances in familial glioma
Chromosome imbalances in familial gliomas detected by comparative genomic hybridization
✍ Niina Paunu; Satu-Leena Sallinen; Ritva Karhu; Helena Miettinen; Pauli Sallinen; 📂 Article 📅 2000 🏛 John Wiley and Sons 🌐 English ⚖ 333 KB 👁 2 views

Familial occurrence of gliomas, in the absence of well-defined hereditary multisystem disorders, is reported occasionally. We describe 17 families that have been afflicted with two or more gliomas but do not raise suspicion of other inheritable syndromes. The families were identified among 369 conse