Und dann auf "Zum Home-Bildschirm [+]".
Stöbern
genialokal zum Startbildschirm hinzufügen
Installieren Sie die genialokal App auf Ihrem Startbildschirm für einen schnellen Zugriff und eine komfortable Nutzung.
Installieren Sie die genialokal App auf Ihrem Startbildschirm für einen schnellen Zugriff und eine komfortable Nutzung.
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
Patrick J. Willems is a former professor of medical genetics at the University of Antwerp, Belgium. He currently is Director of GENDIA, Antwerp, Belgium, a network of laboratories offering genetic testing. He has published over 200 articles in internationally distinguished journals including Cell, Nature Genetics and The New England Journal of Medicine, with many on genetic hearing loss. Dr. Willems received the M.D. and Ph.D. degrees from the University of Antwerp, Belgium.
Preface, Contributors, 1. Normal Development of the Ear in the Human and Mouse, 2. Audiometric Tests and Diagnostic Workup, 3. Classification and Epidemiology, 4. Usher Syndrome, 5. Pendred Syndrome, 6. Waardenburg Syndrome, 7. Jervell and Lange-Nielsen Syndrome, 8. HDR Syndrome, 9. Branchio-oto-renal Syndrome, 10. Treacher Collins Syndrome, 11. MYH9, 12. Mitochondrial Hearing Loss, 13. Gene Localization and Isolation in Nonsyndromic Hearing Loss, 14. Connexins, 15. Myosin VI, 16. K+-Channel Gene KCNQ4, 17. COL11A2, 18. POU-Domain Transcription Factors, 19. a-Tectorin, 20. EYA4, 21. DFNA5, 22. COCH, 23. Diaphanous, 24. Claudin 14, 25. CDH23, 26. TMPRSS3, 27. Otosclerosis, 28. Mechanisms that Regulate Hair Cell Differentiation and Regeneration, 29. Genetic Testing: Possibilities and Attitudes, Index
