3p21

BACKGROUND Findings from family and twin studies suggest that genetic contributions to psychiatric disorders do not in all cases… (More)

BACKGROUND Two inflammatory disorders, type 1 diabetes and celiac disease, cosegregate in populations, suggesting a common… (More)

Nasopharyngeal carcinoma (NPC) poses one of the serious health problems in southern Chinese, with an incidence rate ranging from… (More)

Allelic loss at the short arm of chromosome 3 is one of the most common and earliest events in the pathogenesis of lung cancer… (More)

Two new members of a family of putative hyaluronidase genes involved in glycosaminoglycan catabolism have been identified and… (More)

The chemokine receptor 5 (CKR5) protein serves as a secondary receptor on CD4(+) T lymphocytes for certain strains of human… (More)

The human DNA mismatch repair gene homologue hMSH2, on chromosome 2p is involved in hereditary non-polyposis colon cancer (HNPCC… (More)

Some cases of hereditary nonpolyposis colorectal cancer (HNPCC) are due to alterations in a mutS-related mismatch repair gene. A… (More)

Cytogenetic abnormalities and high-frequency allele losses involving the short arm of human chromosome 3 have been identified in… (More)

In childhood malignancies such as retinoblastoma and Wilms tumour, of which both familial and sporadic forms exist, recessive… (More)