15q21

A genome-wide association study was performed to identify genetic factors involved in susceptibility to psoriasis (PS) and… Expand

Dyslexia has been linked to a number of chromosomal regions including 15q. Recently a gene, EKN1, with unknown function in the… Expand

Approximately 3–10% of people have specific difficulties in reading, despite adequate intelligence, education, and social… Expand

The neuronal ceroid lipofuscinoses (NCLs) are a group of autosomal recessive neurodegenerative diseases characterized by the… Expand

Normal pigmentation depends on the uniform distribution of melanin-containing vesicles, the melanosomes, in the epidermis… Expand

Griscelli syndrome (GS, MIM 214450), a rare, autosomal recessive disorder, results in pigmentary dilution of the skin and the… Expand

Griscelli syndrome is a rare autosomal recessive disease characterized by pigment dilution, variable cellular immunodeficiency… Expand

Griscelli disease (OMIM 214450) is a rare autosomal recessive disorder characterized by pigmentary dilution, variable cellular… Expand

The childhood neuronal ceroid lipofuscinoses (NCLs) are a group of autosomal recessive neurodegenerative disorders characterised… Expand

We have used cDNA probes for lipoprotein lipase and hepatic lipase to determine the chromosomal and subchromosomal locations of… Expand