2q33-q34

Background: Multiple genome-wide and candidate gene association studies have been conducted in search of common risk variants for… Expand

Background Despite extensive research on the genetic determinants of glaucoma, the genes identified to date explain only a small… Expand

We describe a unique family with two children having a delay in psychomotor development. In both children we identified an… Expand

Amyotrophic lateral sclerosis is a progressive neurodegenerative disease that manifests as selective upper and lower motor neuron… Expand

The human DAZ (deleted in azoospermia) gene family on the Y chromosome and an autosomal DAZ-like gene, DAZL1, encode RNA-binding… Expand

The current paucity of cytogenetic information on hepatocellular carcinoma (HCC) reflects the difficulties in culturing… Expand

The autosomal recessive form of juvenile amyotrophic lateral sclerosis (ALS2; RFALS Type 3) has previously been mapped to the 8… Expand

Using fluorescence in situ hybridization (FISH), we have identified seven NF1-related loci, two separate loci on chromosome 2, at… Expand

The insulin-like growth factor binding proteins (IGFBPs) constitute a structurally related protein family with six known members… Expand

In extracellular fluids the insulin-like growth factors (IGFs) are bound to specific binding proteins (IGBPs). The genes for two… Expand