標題: Titlebook: Genetics and Auditory Disorders; Bronya J. B. Keats,Richard R. Fay,Arthur N. Popper Book 2002 Springer Science+Business Media New York 200 [打印本頁] 作者: hector 時間: 2025-3-21 19:01
書目名稱Genetics and Auditory Disorders影響因子(影響力)
書目名稱Genetics and Auditory Disorders影響因子(影響力)學科排名
書目名稱Genetics and Auditory Disorders網(wǎng)絡公開度
書目名稱Genetics and Auditory Disorders網(wǎng)絡公開度學科排名
書目名稱Genetics and Auditory Disorders被引頻次
書目名稱Genetics and Auditory Disorders被引頻次學科排名
書目名稱Genetics and Auditory Disorders年度引用
書目名稱Genetics and Auditory Disorders年度引用學科排名
書目名稱Genetics and Auditory Disorders讀者反饋
書目名稱Genetics and Auditory Disorders讀者反饋學科排名
作者: 商業(yè)上 時間: 2025-3-21 23:08 作者: Phagocytes 時間: 2025-3-22 00:33
0947-2657 the hearing impaired. Approaches to the diagnosis and treatment of hearing impairment have developed from technological advances in genetic research. This volume covers gene expression, mutations, mapping and cloning, as well as mitochondrial and cellular genetics. Chapters are also included on the 作者: Coma704 時間: 2025-3-22 07:59 作者: hair-bulb 時間: 2025-3-22 10:33 作者: sigmoid-colon 時間: 2025-3-22 15:37
0947-2657 uses of mouse models, genetic epidemiology and genetic counseling specifically for hearing impairment. As a comprehensive review of the genetics of hearing, this book will interest hearing researchers, clinicians and genetic counselors.978-1-4419-3129-0978-0-387-21853-3Series ISSN 0947-2657 Series E-ISSN 2197-1897 作者: sigmoid-colon 時間: 2025-3-22 17:55 作者: 抗原 時間: 2025-3-23 00:48
Autosomal and X-Linked Auditory Disorders,urther characterization of the genes for hearing loss will provide a clearer vision of the structure and function of the auditory system in health and disease. It is hoped that these discoveries will establish a conceptual basis for the rational therapy of hearing loss and deafness.作者: 變白 時間: 2025-3-23 01:47 作者: 按等級 時間: 2025-3-23 08:36
https://doi.org/10.1007/978-3-322-98943-7l hearing impairment have resulted in mapping of 30 autosomal dominant, 28 autosomal recessive and 5 X-linked loci for nonsyndromic hearing impairment. Physical mapping and the use of a variety of cloning approaches over the same time period have led to the identification of 18 of these genes. Furth作者: 嚴厲批評 時間: 2025-3-23 13:01 作者: STEER 時間: 2025-3-23 14:16 作者: 漂浮 時間: 2025-3-23 21:01
Der Kampf um den verlorenen Tagt degrees of severity. These mutations are not uncommon and, owing to the susceptibility of individuals with the A1555G and ΔT961Cn mutations and their maternal relatives to aminoglycosides, are important to diagnose. Despite the fact that these mostly homoplasmic mitochondrial mutations represent t作者: DNR215 時間: 2025-3-23 22:25
Die Krisis der s?kularen Religionen mutants will all contribute to our growing understanding of the complexity of deafness. Many more mouse mutants are candidates for involvement of the auditory system, but their hearing has not yet been investigated in any detail. Some of these are listed in additional tables available at the Web si作者: sebaceous-gland 時間: 2025-3-24 05:07
https://doi.org/10.1007/978-3-662-26431-7ve, supportive, and sensitive to the special needs of individuals. Professionals who provide health care and services to deaf and hard of hearing children and adults are essential to the referral process. Genetic counseling includes the collection of medical and family history information, a physica作者: Pcos971 時間: 2025-3-24 07:24 作者: Anticoagulant 時間: 2025-3-24 13:13 作者: 軟膏 時間: 2025-3-24 16:51
Genetics and Auditory Disorders978-0-387-21853-3Series ISSN 0947-2657 Series E-ISSN 2197-1897 作者: objection 時間: 2025-3-24 20:21 作者: elastic 時間: 2025-3-24 23:19
,W?hlen im Schatten der Pandemie,nslocation. The advantage would be that, if such a chromosome rearrangement were found, it would immediately suggest the location of the deafness gene..The cochlear ESTs and libraries that exist have been extremely helpful in understanding different aspects of the molecular biology of the inner ear.作者: 清晰 時間: 2025-3-25 06:37
Der Kampf um den verlorenen Tagusing spontaneous mouse models of mitochondrial hearing impairment, or direct investigation of the most likely biochemical pathways involved, may help not only in elucidating the pathophysiology between mtDNA mutations and hearing loss, but may also provide a paradigm for mitochondrial diseases in g作者: Ostrich 時間: 2025-3-25 09:20 作者: Decongestant 時間: 2025-3-25 12:07 作者: Obvious 時間: 2025-3-25 18:35
Introduction and Overview: Genetics in Auditory Science and Clinical Audiology,作者: 博愛家 時間: 2025-3-25 23:46 作者: 騙子 時間: 2025-3-26 00:37
Mapping and Cloning of Genes for Inherited Hearing Impairment,ssion, audiological configuration, etc.), the description of the phenotype should include documentation of the presence or absence of associated vestibular abnormalities, and/or neuroradiological findings in the inner ear. By this means, the results of the research findings will rapidly translate in作者: 瘋狂 時間: 2025-3-26 05:07
Cytogenetics and Cochlear Expressed Sequence Tags (ESTs) for Identification of Genes Involved in Henslocation. The advantage would be that, if such a chromosome rearrangement were found, it would immediately suggest the location of the deafness gene..The cochlear ESTs and libraries that exist have been extremely helpful in understanding different aspects of the molecular biology of the inner ear.作者: 手榴彈 時間: 2025-3-26 08:30
Hearing Loss and Mitochondrial DNA Mutations: Clinical Implications and Biological Lessons,using spontaneous mouse models of mitochondrial hearing impairment, or direct investigation of the most likely biochemical pathways involved, may help not only in elucidating the pathophysiology between mtDNA mutations and hearing loss, but may also provide a paradigm for mitochondrial diseases in g作者: 污點 時間: 2025-3-26 14:23
Mice as Models for Human Hereditary Deafness,to fill the gap between human deafness and mouse models (Nolan et al. 2000). Large-scale, genome-wide mutagenesis programmes are starting in other countries too, including the US, so there will soon be many more mutants available. Deafness is one of the most heterogeneous diseases known in humans, a作者: 遭遇 時間: 2025-3-26 17:48 作者: jabber 時間: 2025-3-26 22:31 作者: 人類學家 時間: 2025-3-27 03:22
Mapping and Cloning of Genes for Inherited Hearing Impairment,l hearing impairment have resulted in mapping of 30 autosomal dominant, 28 autosomal recessive and 5 X-linked loci for nonsyndromic hearing impairment. Physical mapping and the use of a variety of cloning approaches over the same time period have led to the identification of 18 of these genes. Furth作者: legacy 時間: 2025-3-27 07:19
Cytogenetics and Cochlear Expressed Sequence Tags (ESTs) for Identification of Genes Involved in Hestudies are costly, and karyotypic anomalies are likely to account for a low percentage of cases. In addition, only a relatively small proportion of molecular biologists have any expertise with cytogenetic techniques. Appropriately, cytogenetics is not the first technique to be considered when evalu作者: insurgent 時間: 2025-3-27 10:32
Autosomal and X-Linked Auditory Disorders,uditory system and its associated electromechanical processes requires the orchestrated temporal and spatial expression of numerous different genes. Further characterization of the genes for hearing loss will provide a clearer vision of the structure and function of the auditory system in health and作者: 顯微鏡 時間: 2025-3-27 16:55
Hearing Loss and Mitochondrial DNA Mutations: Clinical Implications and Biological Lessons,t degrees of severity. These mutations are not uncommon and, owing to the susceptibility of individuals with the A1555G and ΔT961Cn mutations and their maternal relatives to aminoglycosides, are important to diagnose. Despite the fact that these mostly homoplasmic mitochondrial mutations represent t作者: 佛刊 時間: 2025-3-27 19:49 作者: 抵押貸款 時間: 2025-3-28 01:51
Genetic Counseling for Deafness,ve, supportive, and sensitive to the special needs of individuals. Professionals who provide health care and services to deaf and hard of hearing children and adults are essential to the referral process. Genetic counseling includes the collection of medical and family history information, a physica作者: Pageant 時間: 2025-3-28 04:55
A First Biopollution Index Approach and Its Relationship on Biological Quality in Catalan Rivers,iven biological element? This discussion will be done in relation to the use of information on alien species (AS) for the purpose of future management and the ensuing role of uncertainty in the ecological assessment on water bodies according to the Water Framework Directive (2000/60/EC).作者: 從容 時間: 2025-3-28 07:34 作者: 公司 時間: 2025-3-28 11:42 作者: TAIN 時間: 2025-3-28 17:30 作者: averse 時間: 2025-3-28 22:47
William Polen, wie Sie das fundamentale Konzept der Erhaltungsgr??en, deren Bilanzen und Str?me anwenden, um L?sungen zu finden, auch zu Fragen im Zusammenhang mit der Energiewende..978-3-662-67905-0978-3-662-67906-7作者: 恃強凌弱的人 時間: 2025-3-29 01:25
2626-224X mploys a longue durée perspective that analyzes contemporary desires and expectations while tracing and placing them inside Tunisia’s history. It thus contributes to our understanding of state-society relations and global capitalism in Tunisia.978-3-658-43869-2978-3-658-43870-8Series ISSN 2626-224X Series E-ISSN 2626-2258 作者: 偽造 時間: 2025-3-29 05:40
n been edited and reviewed by a medical student with a special interest in the topic. This near-peer style of writing allows our content to cater to a student’s needs at the right level, whilst having the expert input of surgeons who are leaders in their field.?.978-3-319-82759-9978-3-319-43210-6作者: JECT 時間: 2025-3-29 10:17
Book 2019mic growth. The ASEAN market is widely regarded as a new hub of growth, not least in light of increasing protectionism and declining economic growth of the three largest countries in Northeast Asia (China, Japan, and South Korea). Contributors address a range of issues with a concentrated focus on e
