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Lethal Mutations
Sunday, April 12, 2009
Chromosomal locations of human deafness genes
Almost every human chromosome harbors at
least one gene involved in nonsyndromic
monogenic hearing loss. The diagrammatic
presentation shown here is limited to nonsyndromic
hearing loss.
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2009
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Genes for photoreceptor proteins in cones
Hearing and Deafness
The main components of the ear
The cochlea
The outer hair cell
Chromosomal locations of human deafness genes
Odorant Receptor Gene Family
Olfactory nerve cells in the nasal mucous membrane
Odor-specific transmembrane receptors and GTP-bind...
Olfactory receptor protein
Assignment of olfactory receptor RNA to neurons
Subfamilies within the multigene family
Mammalian Taste Receptor Gene Family
Mammalian chemosensory epithelia
Mammalian chemosensory system
Taste receptor gene family
Expression of many taste receptor genes in the sam...
Genes in Embryonic Development
The segmental organization of the fruit fly (Droso...
Embryonic lethal mutations
Examples of developmental mutants
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