Genetics Evaluation Guidelines for the Etiologic Diagnosis of Congenital Hearing Loss
- 1 May 2002
- journal article
- guideline
- Published by Elsevier BV in Genetics in Medicine
- Vol. 4 (3), 162-171
- https://doi.org/10.1097/00125817-200205000-00011
Abstract
No abstract availableThis publication has 28 references indexed in Scilit:
- At the Speed of Sound: Gene Discovery in the Auditory SystemAmerican Journal of Human Genetics, 2001
- Parental Attitudes toward Genetic Testing for Pediatric DeafnessAmerican Journal of Human Genetics, 2000
- Year 2000 Position Statement: Principles and Guidelines for Early Hearing Detection and Intervention ProgramsPEDIATRICS, 2000
- Assessment of Stress in Mothers of Children With Severe Breath-Holding SpellsPEDIATRICS, 2000
- Statement of the American College of Medical Genetics on Universal Newborn Hearing ScreeningGenetics in Medicine, 2000
- Heterogenous Point Mutations in the Mitochondrial tRNA Ser(UCN) Precursor Coexisting with the A1555G Mutation in Deaf Students from MongoliaAmerican Journal of Human Genetics, 1999
- Attitudes of Deaf Adults toward Genetic Testing for Hereditary DeafnessAmerican Journal of Human Genetics, 1998
- Familial Progressive Sensorineural Deafness Is Mainly Due to the mtDNA A1555G Mutation and Is Enhanced by Treatment with AminoglycosidesAmerican Journal of Human Genetics, 1998
- The Genetic Privacy Act: An Analysis of Privacy and Research ConcernsThe Journal of Law, Medicine & Ethics, 1997
- Genetic Epidemiology of Hearing ImpairmentAnnals of the New York Academy of Sciences, 1991