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Genetic Hearing Loss, Hardcover by Willems, Patrick J. (EDT), Brand New, Free...
US $305.73
ApproximatelyAU $459.16
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Located in: Jessup, Maryland, United States
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Estimated between Thu, 11 Jul and Mon, 22 Jul to 43230
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eBay item number:364848038232
Item specifics
- Condition
- Book Title
- Genetic Hearing Loss
- ISBN
- 9780824743093
- Subject Area
- Science, Medical
- Publication Name
- Genetic Hearing Loss
- Publisher
- CRC Press LLC
- Item Length
- 9.3 in
- Subject
- Life Sciences / Molecular Biology, Audiology & Speech Pathology, Genetics, General
- Publication Year
- 2003
- Type
- Textbook
- Format
- Hardcover
- Language
- English
- Item Height
- 1.1 in
- Item Weight
- 28.2 Oz
- Item Width
- 6.2 in
- Number of Pages
- 406 Pages
About this product
Product Information
Genetic Hearing Loss branches into syndromic and nonsyndromic categorical directions in its coverage of the genetics behind hearing loss.
Product Identifiers
Publisher
CRC Press LLC
ISBN-10
0824743091
ISBN-13
9780824743093
eBay Product ID (ePID)
30284712
Product Key Features
Number of Pages
406 Pages
Language
English
Publication Name
Genetic Hearing Loss
Publication Year
2003
Subject
Life Sciences / Molecular Biology, Audiology & Speech Pathology, Genetics, General
Type
Textbook
Subject Area
Science, Medical
Format
Hardcover
Dimensions
Item Height
1.1 in
Item Weight
28.2 Oz
Item Length
9.3 in
Item Width
6.2 in
Additional Product Features
Intended Audience
Scholarly & Professional
LCCN
2003-062467
Dewey Edition
22
Illustrated
Yes
Dewey Decimal
617.8/042
Lc Classification Number
Rf292.G455 2004
Table of Content
Hearing and hearing loss: normal development of the ear in the human and mouse, audiometric tests and diagnostic workup, classification and epidemiology of hearing loss, Syndromic hearing loss: Usher syndrome, pendred syndrome, Waardenburg syndrome, Nielsensyndrome, HDR syndrome, branchio-oto-renal syndrome, Treacher Collins syndrome, MYH9, mitochondrial hearingloss, Genes responsible for nonsyndromic hearing loss: gene localization and isolation in nonsyndromic hearing loss, connexins, myosin VI, K+ channel gene KCNQ4, COL11A2, POU-Domain transcription factors, a-Tectorin P. EYA4 DFNA 5 COCH Diaphanous, Claudin 14 CDH23 TMPRSS33, otosclerosis. Miscellaneous factors: mechanisms that regulate hair cell differentiation and regeneration, genetic testing - possibilitiesand attitudes.
Copyright Date
2004
Item description from the seller
Seller assumes all responsibility for this listing.
eBay item number:364848038232
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Jessup, Maryland, United States
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