DFNB15: autosomal recessive non-syndromic hearing loss gene-chromosome 3q, 19p or digenic recessive inheritance? 2000

A H Chen, and K Fukushima, and W T McGuirt, and R J Smith
Department of Otolaryngology, Head and Neck Surgery, University of Iowa, Iowa City, USA.

UI MeSH Term Description Entries
D008040 Genetic Linkage The co-inheritance of two or more non-allelic GENES due to their being located more or less closely on the same CHROMOSOME. Genetic Linkage Analysis,Linkage, Genetic,Analyses, Genetic Linkage,Analysis, Genetic Linkage,Genetic Linkage Analyses,Linkage Analyses, Genetic,Linkage Analysis, Genetic
D002874 Chromosome Mapping Any method used for determining the location of and relative distances between genes on a chromosome. Gene Mapping,Linkage Mapping,Genome Mapping,Chromosome Mappings,Gene Mappings,Genome Mappings,Linkage Mappings,Mapping, Chromosome,Mapping, Gene,Mapping, Genome,Mapping, Linkage,Mappings, Chromosome,Mappings, Gene,Mappings, Genome,Mappings, Linkage
D002888 Chromosomes, Human, Pair 19 A specific pair of GROUP F CHROMOSOMES of the human chromosome classification. Chromosome 19
D002893 Chromosomes, Human, Pair 3 A specific pair of human chromosomes in group A (CHROMOSOMES, HUMAN, 1-3) of the human chromosome classification. Chromosome 3
D003638 Deafness A general term for the complete loss of the ability to hear from both ears. Deafness Permanent,Hearing Loss Permanent,Prelingual Deafness,Deaf Mutism,Deaf-Mutism,Deafness, Acquired,Hearing Loss, Complete,Hearing Loss, Extreme,Acquired Deafness,Complete Hearing Loss,Deafness, Prelingual,Extreme Hearing Loss,Permanent, Deafness,Permanent, Hearing Loss,Permanents, Deafness
D005808 Genes, Recessive Genes that influence the PHENOTYPE only in the homozygous state. Conditions, Recessive Genetic,Genetic Conditions, Recessive,Recessive Genetic Conditions,Condition, Recessive Genetic,Gene, Recessive,Genetic Condition, Recessive,Recessive Gene,Recessive Genes,Recessive Genetic Condition
D006319 Hearing Loss, Sensorineural Hearing loss resulting from damage to the COCHLEA and the sensorineural elements which lie internally beyond the oval and round windows. These elements include the AUDITORY NERVE and its connections in the BRAINSTEM. Deafness Neurosensory,Deafness, Neurosensory,Deafness, Sensoryneural,Neurosensory Deafness,Sensorineural Hearing Loss,Sensoryneural Deafness,Cochlear Hearing Loss,Hearing Loss, Cochlear,Deafnesses, Neurosensory,Deafnesses, Sensoryneural,Neurosensory Deafnesses,Sensoryneural Deafness,Sensoryneural Deafnesses
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man

Related Publications

A H Chen, and K Fukushima, and W T McGuirt, and R J Smith
September 1997, American journal of medical genetics,
A H Chen, and K Fukushima, and W T McGuirt, and R J Smith
February 2013, International journal of pediatric otorhinolaryngology,
A H Chen, and K Fukushima, and W T McGuirt, and R J Smith
December 2019, European journal of medical genetics,
A H Chen, and K Fukushima, and W T McGuirt, and R J Smith
September 2019, Turkish archives of otorhinolaryngology,
A H Chen, and K Fukushima, and W T McGuirt, and R J Smith
January 2014, PloS one,
A H Chen, and K Fukushima, and W T McGuirt, and R J Smith
November 2015, International journal of pediatric otorhinolaryngology,
A H Chen, and K Fukushima, and W T McGuirt, and R J Smith
May 2002, Human mutation,
A H Chen, and K Fukushima, and W T McGuirt, and R J Smith
July 1996, Acta oto-laryngologica,
A H Chen, and K Fukushima, and W T McGuirt, and R J Smith
March 1985, International journal of pediatric otorhinolaryngology,
Copied contents to your clipboard!