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Genetic Hearing Loss
Heredity, either alone or in combination with environmental factors, is the most prominent underlying cause of hearing impairment. Thanks in large part to positional cloning techniques, scientists have identified nearly 100 gene loci implicated in hearing loss since 1995-an extraordinarily rapid rate of gene identification. Genetic Hearing Loss
Genetic Hearing Loss
Heredity, either alone or in combination with environmental factors, is the most prominent underlying cause of hearing impairment. Thanks in large part to positional cloning techniques, scientists have identified nearly 100 gene loci implicated in hearing loss since 1995-an extraordinarily rapid rate of gene identification. Genetic Hearing Loss branches into syndromic and nonsyndromic categorical directions in its coverage of the genetics behind hearing loss. Authored by 60 internationally recognized researchers, the book describes the normal development of the ear, updates the classification and epidemiology of hearing loss, and surveys the usage of audiometric tests and diagnostic medical examinations.
Ear, Nose, and Throat
The interconnectedness of the ear, nose, and throat is evident when you consider how the smell of garlic cloves on the grill or chocolate chip cookies in the oven can affect your perception of their taste, or how a runny nose and scratchy throat can lead to an ear infection. In addition to enabling sensory perception, the ear, nose, and throat perform a number of vital functions in the human body. This incisive volume examines the structure of each in turn and in concert with the other, also exploring the diseases and disorders that sometimes afflict them.
Human Genome Methods
Human Genome Methods is a practical guide to the application of molecular biology and genetics techniques to research on human cells. Written by recognized authorities who often originated the techniques described, chapters present experimental protocols that are readily used at the laboratory bench. The step-by-step protocols are concise and easy to follow to be reproducible by researchers of various levels of expertise. Suggestions for successful application of procedures are included, along with recommended materials and suppliers. Helpful background information and results of applying the methods described are also given. Section I covers topics such as microsatellite DNA, dynamic mutati...
Statement of Disbursements of the House as Compiled by the Chief Administrative Officer from ...
Covers receipts and expenditures of appropriations and other funds.
The Episcopal Church Annual 2023
The leading source of information on the Episcopal Church With origins dating back to 1830, The Episcopal Church Annual - aka "The Red Book" - is an indispensable reference tool, trusted year-after-year by churches, diocesan offices, libraries, and many others. You will find the following between the covers of the 2023 edition of "The Red Book", and more: - A comprehensive directory of provinces, dioceses, and churches, including contact information and listings of active clergy - The canonical structure and organization of the Episcopal Church, including complete directories for the Office of The General Convention, The House of Bishops, The House of Deputies, standing committees and commissions, and more - Listings and contact information for seminaries; Episcopal schools; centers for camps, conferences, and retreats; Episcopal Church Women; and more - Up-to-date church-wide statistical data and chronological tables - A classified buyer's guide of vendors and organizations offering valued services to the church
Genetics and Hearing Impairment
The aim of this book is to provide a description of what is currently known about the genetics of deafness for audiologists, otologists and general genetics. It includes a number of background chapters introducing relevant genetics for audiologists and otologists and relevant aspects of auditory intervention for geneticists. These cover the epidemiology of hearing loss and the current situation with regard to gene identification within the field. Chapters on the common syndromes, eg Ushers, Waardenburg, Pendred, Branchio-otorenal and Treacher Collins are followed by coverage of Dominant, Recessive and x-linked non-syndromal deafness, together with mitrochondial deafness. The final section includes chapters on the genetic, rehabilitative and surgical management of genetic disorders.
