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101 0 $aeng
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181   $ctxt$2rdacontent
182   $cc$2rdamedia
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200 00$aHereditary hearing loss and its syndromes /$fedited by Helga V. Toriello, Shelley D. Smith
205   $a3rd ed.
210   $aOxford, England $cOxford University Press$dc2013
215   $a1 online resource (xiv, 732 p.) $cill
225 1 $aOxford Monographs on Medical Genetics ;$v63
311   $a0-19-973196-9 
311   $a1-299-70888-9 
320   $aIncludes bibliographical references at the end of each chapters and index.
327   $aGenetic hearing loss : a brief history -- Epidemiology, etiology, genetic mechanisms, and genetic counseling -- Embryology of the mammalian ear -- Gene/environment interactions in acquired hearing loss -- Syndrome diagnosis and investigation in the hearing-impaired patient -- Genetic hearing loss with no associated abnormities -- Genetic hearing loss associated with external ear abnormalities -- Eye disorders -- Genetic hearing loss associated with musculoskeletal disorders -- Genetic hearing loss associated with renal disorders -- Genetic hearing loss associated with neurologic and neuromuscular disorders -- Genetics hearing loss associated with cardiac abnormalities -- Genetic hearing loss associated with endocrine disorders -- Genetic hearing loss associated with metabolic disorders -- Integumentary disorders -- Oral and dental disorderss -- Chromosome disorders.
330   $aThis is the third edition of the foremost medical reference on genetic hearing loss, updated to include new information on molecular mechanisms. It is an excellent resource for physicians, audiologists, and other professionals working with individuals with hearing loss and their families, and for clinical training programs and researchers in hearing sciences.
410  0$aOxford monographs on medical genetics ;$vno. 63.
606   $aHearing disorders
606   $aDeafness$xGenetic aspects
615  0$aHearing disorders.
615  0$aDeafness$xGenetic aspects.
676   $a617.8
701   $aToriello$b Helga V$01609494
701   $aSmith$b Shelley D.$f1949-$01609495
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906   $aBOOK
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996   $aHereditary hearing loss and its syndromes$93936781
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