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To identify genetic susceptibility loci for nasopharyngeal carcinoma (NPC), a genome-wide association study was performed using… Expand Mutations within the FMS-like tyrosine kinase 3 (FLT3) gene on chromosome 13q12 have been detected in up to 35% of acute myeloid… Expand Hearing impairment is a common and highly heterogeneous sensory disorder. Genetic causes are thought to be responsible for more… Expand The purpose of this study was to assess 65 pedigrees ascertained through a Bipolar I (BPI) proband for evidence of linkage, using… Expand BACKGROUND
Inherited hearing impairment affects about 1 in 2000 newborns. Up to 50 percent of all patients with autosomal… Expand factors1. Mutations in the connexin26 gene (GJB2), located on 13q12, are responsible for non-syndromic recessive and dominant… Expand Inactivation of the klotho (kl) gene in mice results in multiple disorders that resemble human aging. The mouse kl gene encodes a… Expand Chromosome studies of lipomas have revealed an extensive cytogenetic heterogeneity. To investigate the frequencies of previously… Expand Non–syndromic, recessively inherited deafness is the most predominant form of severe inherited childhood deafness. Until now, no… Expand Research in oncogenetics has led to the identification of two major classes of tumor‐associated genes, oncogenes and tumor… Expand