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Hereditary Hearing Loss and Its Syndromes (Oxford Monographs on Medical Genetics, No. 50)

Hereditary Hearing Loss and Its Syndromes (Oxford Monographs on Medical Genetics, No. 50)

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Creators: Helga V. Toriello, William Reardon, Robert J. Gorlin
Publisher: Oxford University Press, USA
Category: Book

List Price: $169.50
Buy New: $141.93
You Save: $27.57 (16%)



New (15) Used (5) from $141.93

Avg. Customer Rating: 5.0 out of 5 stars 1 reviews
Sales Rank: 762992

Media: Hardcover
Edition: 2
Number Of Items: 1
Pages: 528
Shipping Weight (lbs): 3.8
Dimensions (in): 11.3 x 8.7 x 1.2

ISBN: 019513849X
Dewey Decimal Number: 617.8042
EAN: 9780195138498
ASIN: 019513849X

Publication Date: February 19, 2004
Availability: Usually ships in 1-2 business days
Condition: Absolutely Brand New & In Stock. 100% 30-Day Money Back. Direct from our warehouse. Ships by USPS. 1+ million customers served-In business since 1986. Happy Customers is Our #1 Goal. Toll Free Support

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  • Hardcover - Hereditary Hearing Loss and Its Syndromes (Oxford Monographs on Medical Genetics)

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Editorial Reviews:

Product Description
Genetic deafness affects 1 in 1000 children, and over the last decade several dozen of the responsible genes have been identified. This unique textbook aims to assist clinicians dealing with deaf patients and families by critically reviewing all relevant published material on genetics, pathology, clinical presentation, diagnosis, and laboratory findings. Thoroughly revised, the Second Edition has been updated throughout and includes a new chapter on hearing loss with cardiovascular disorders. It continues with the successful formula of presenting separate chapters on deafness associated with findings in specific body systems. Careful attention to cross referencing between chapters means that the multifaceted clinical presentations of distinct conditions are highlighted. These clinical variations are complemented by excellent clinical photographs, audiograms, figures from essential laboratory or other investigations, and comprehensive reference lists. Gene mutations that cause deafness are highlighted throughout the text, both in chapters dealing with syndromes and in a vastly expanded chapter focusing specifically on nonsyndromic forms of deafness. Thus, the new edition reflects all the progress on the molecular understanding of deafness made in recent years and integrates these findings into clinical practice. It also makes an important contribution to the cataloguing of new syndromes that have emerged in recent years, such as HIDS and X-linked maxillofacial dysostosis.


Customer Reviews:

5 out of 5 stars My Favorite Book   May 5, 2001
 2 out of 2 found this review helpful

It is the best book that exists for consultation on genetic syndromic hearing loss, since in very organized form it treats the audiologic aspects perfectly and genetic of these syndromes.It is my favorite book and I recommend it to you if you are geneticist or audiologist.

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