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OverviewDeafness is a hearing impairment and can be classified as genetic or acquired, pre-lingual or post-lingual and syndromic or non-syndromic. This book contains details of materials, methods, literature, results and other information which will enable to study the linkage of genetic deafness. Consanguineous families of different ethnic groups having deaf individuals were studied. Pedigrees were drawn of all families having three or more affected members and showed recessive mode of inheritance. DNA was extracted from blood samples. Short Tandem Repeat markers for DFNB3 locus were amplified using PCR and genotyped for identification of hereditary hearing loss due to DFNB3 in Pakistani families Full Product DetailsAuthor: Ali Akhtar , Babar Masroor EllahiPublisher: LAP Lambert Academic Publishing Imprint: LAP Lambert Academic Publishing Dimensions: Width: 15.20cm , Height: 0.50cm , Length: 22.90cm Weight: 0.122kg ISBN: 9783659377631ISBN 10: 3659377635 Pages: 76 Publication Date: 01 April 2013 Audience: General/trade , General Format: Paperback Publisher's Status: Active Availability: In stock  We have confirmation that this item is in stock with the supplier. It will be ordered in for you and dispatched immediately. Table of ContentsReviewsAuthor InformationTab Content 6Author Website:Countries AvailableAll regions |
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