Terminal osseous dysplasia
Terminal osseous dysplasia (TOD) is a rare genetic condition that affects the development of bones, specifically in the hands, feet, and face.…
TAF1 gene
The TAF1 gene, also known as TAF1Dyt3, is a critical gene involved in transcription. It is located in a region near other…
RNASEH2C gene
The RNASEH2C gene is an important gene associated with a group of genetic disorders known as Aicardi-Goutières Syndrome (AGS). AGS is a…
Drug Use Screening Tests
Drug abuse is a serious issue that affects individuals of all ages. Many people, alone or with friends, find themselves abusing substances,…
Juvenile Paget disease
Paget’s disease of bone (PDB) is a rare genetic disorder that affects the bones in the body. It is also known as…
HSPB8 gene
The HSPB8 gene, also known as HSP22, is a gene that is associated with various neurological conditions, including neuropathy and Charcot-Marie-Tooth disease.…
Genes J
Genes J is a scientific journal dedicated to the study of genetics. It provides a platform for researchers and scientists to publish…
Epithelial Cells in Urine
Epithelial cells are the cells that make up the outer surface of the body, including the skin and the lining of certain…
FAM83H gene
The FAM83H gene is a genetic gene that has been found to be associated with several conditions. It is listed in various…