Sprenger, S H <br/><br/>
Characteristic chromosomal aberrations in sporadic cerebellar hemangioblastomas revealed by comparative genomic hybridization.  [electronic resource] 

 -  Journal of neuro-oncology  May 2001 
 - 241-7 p.  digital 
<br/><br/> Publication Type: Comparative Study; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0167-594X 
<br/><br/><label>Standard No.: </label>10.1023/a:1010623119469  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adrenal Gland Neoplasms--genetics<br/>Adult<br/>Aged<br/>Carcinoma, Renal Cell--genetics<br/>Cell Transformation, Neoplastic--genetics<br/>Cerebellar Neoplasms--genetics<br/>Chromosome Aberrations<br/>Chromosomes, Human, Pair 18--ultrastructure<br/>Chromosomes, Human, Pair 19<br/>Chromosomes, Human, Pair 3--genetics<br/>Chromosomes, Human, Pair 6<br/>Chromosomes, Human, Pair 9<br/>DNA, Neoplasm--genetics<br/>Hemangioblastoma--genetics<br/>Humans<br/>Kidney Neoplasms--genetics<br/>Ligases--deficiency<br/>Loss of Heterozygosity<br/>Middle Aged<br/>Monosomy<br/>Nucleic Acid Hybridization<br/>Pheochromocytoma--genetics<br/>Trisomy<br/>Tumor Suppressor Proteins<br/>Ubiquitin-Protein Ligases<br/>Von Hippel-Lindau Tumor Suppressor Protein<br/>von Hippel-Lindau Disease--genetics