Chromosome 9 Short Arm

Somatic alterations of the lymphoid transcription factor gene PAX5 (also known as BSAP) are a hallmark of B cell precursor acute… Expand

Several families have been reported with autosomal-dominant frontotemporal dementia (FTD) and amyotrophic lateral sclerosis (ALS… Expand

BACKGROUND The genetic cause of amyotrophic lateral sclerosis (ALS) is not well understood. Finland is a well suited location for… Expand

Genome-wide association studies have identified a region on chromosome 9p that is associated with coronary artery disease (CAD… Expand

Stroke is the world's third leading cause of death. One cause of stroke, intracranial aneurysm, affects ∼2% of the population and… Expand

Loss of heterozygosity (LOH), either with or without accompanying copy-number loss, is a cardinal feature of cancer genomes that… Expand

The only molecular similarity in sex determination found so far among phyla is between the Drosophila doublesex (dsx) and… Expand

Comparative genomic hybridization was applied for a comprehensive screening of frequently occurring net gains and losses of… Expand

Identification of genetic alterations in bladder cancer is proceeding very rapidly. The most common genetic alteration identified… Expand

A locus for familial melanoma, MLM, has been mapped within the same interval on chromosome 9p21 as the gene for a putative cell… Expand