Presymptomatic diagnosis of nonsyndromic hearing loss by genotyping

Archives of Otolaryngology - Head and Neck Surgery

Volumn 124, Issue 1, 1998, Pages 20-24

  Chen, Achih H ^a   Mueller, Robert F ^b   Prasad, Sai D ^a   Greinwald Jr , John H ^a   Manaligod, Jose ^a   Muilenburg, Ann C ^a   Verhoeven, Kristien ^c   Van Camp, Guy ^c   Smith, Richard J H ^a  

^a UNIVERSITY OF IOWA   (United States)

^b ST JAMES S UNIVERSITY HOSPITAL   (United Kingdom)

^c UNIVERSITY OF ANTWERP   (Belgium)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CHROMOSOME 19; CHROMOSOME 6; GENETIC COUNSELING; GENETIC LINKAGE; GENOTYPE; HAPLOTYPE; HEARING LOSS; HUMAN; MOLECULAR CLONING; PRENATAL DIAGNOSIS; TANDEM REPEAT;

EID: 0031910276     PISSN: 08864470     EISSN: None     Source Type: Journal    
DOI: 10.1001/archotol.124.1.20     Document Type: Article

References (25)

1. Fraser GR. Sex-linked recessive congenital deafness and the excess of males in profound childhood deafness. Am Hum Genet. 1964;29:171-196.
2. Morton NE. Genetic epidemiology of hearing impairment. Ann N Y Acad Sci. 1991; 630:16-31.
3. Roberts J. Hearing Status and Ear Examination: Findings Among Adults in the United States, 1960-1962. Rockville, Md: National Center for Health Studies; 1968. Report-Series II, No. 32.
4. McKusick VA. Mendelian Inheritance in Man. 10th ed. Baltimore, Md: Johns Hopkins University Press; 1992.
5. Fraser GR. The Causes of Profound Deafness in Childhood. Baltimore, Md: Johns Hopkins University Press; 1976.
6. Rosner B. Fundamentals of Biostatistics. Boston, Mass: PWS-Kent Publishing Co; 1990.
7. Ott J. Analysis of Human Genetic Linkage. Baltimore, Md: Johns Hopkins University Press; 1985.
8. Jorde LB, Carey JC, White RL. Medical Genetics. St Louis, Mo: Mosby-Year Book Inc; 1995:129-135.
9. Terwilliger JD, Ott J. Handbook of Human Genetic Linkage. Baltimore, Md: Johns Hopkins University Press; 1994:4-8.
10. Conneally PM, Rivas ML. Linkage analysis in man. In: Advances in Human Genetics. New York, NY: Plenum Publishing Corp; 1985;10:356-360.
11. Chen AH, Ni L, Fukushima K, et al. Linkage of a gene for dominant non-syndromic deafness to chromosome 19. Hum Mol Genet. 1995;4:1073-1076.
12. O'Neill M, Marietta J, Nishimura D, et al. A gene for autosomal dominant non-syndromic hearing loss, DFNA10, maps to chromosome 6. Hum Mol Genet. 1996; 5:853-856.
13. Ad Hoc Committee on Genetic Counseling. Genetic counseling. Am J Hum Genet. 1975;27:240-242.
14. Lindhout D, Frets PG, Niermeijer MF. Approaches to genetic counseling. Ann N Y Acad Sci. 1991;630:223-229.
15. Mueller RF. Genetic counseling for hearing impairment. In: Genetics and Hearing Impairment. London, England: Whurr Publishers; 1996:255-264.
16. Keisell DP, Dunlop J, Stevens HP, et al. Connexin 26 mutations in hereditary non-syndromic sensorineural deafness. Nature. 1997;387:80-83.
17. Liu XZ, Walsh J, Mburu P, et al. Mutations in the myosin VIIA gene cause non-syndromic recessive deafness. Nat Genet. 1997;16:188-190.
18. Weil D, Kussel P, Blanchard S, et al. The autosomal recessive isolated deafness, DFNB2, and the Usher1 B syndrome are allelic defects of the myosin-VIIA gene. Nat Genet. 1997;16:191-193.
19. Turner JH. Legal and social issues in medical genetics. Am J Obstet Gynecol. 1979;134:83-99.
20. International Huntington Association and World Federation of Neurology. Ethical issues policy statement on Huntington's disease molecular genetics predictive test. J Med Genet. 1990;27:34-38.
21. Council on Ethical and Judicial Affairs. Code of Medical Ethics: Current Opinions With Annotations. 150th ed. Chicago, III: American Medical Association; 1997.
22. Andersson Y. Sociological implications of genetic deafness. Am J Hum Genet. 1991;49(suppl):5.
23. Arnos KS, Cunningham M, Israel J, Marazita ML. Innovative approach to genetic counseling services for the deaf population. Am J Med Genet. 1992;44: 345-351.
24. Jordan IK. Ethical issues in the genetic study of deafness. Ann N Y Acad Sci. 1991;630:236-239.
25. Arnos KS, Isreal J, Cunningham M. A model program for genetic counseling of the deaf. Ann N Y Acad Sci. 1991;630:317-318.