2q33-q34

BACKGROUND Multiple genome-wide and candidate gene association studies have been conducted in search of common risk variants for… (More)

BACKGROUND Despite extensive research on the genetic determinants of glaucoma, the genes identified to date explain only a small… (More)

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

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

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

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

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

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

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

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