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. 1995 Oct;57(4):965–968.

Nonsyndromic autosomal recessive deafness is linked to the DFNB1 locus in a large inbred Bedouin family from Israel.

D A Scott, R Carmi, K Elbedour, G M Duyk, E M Stone, V C Sheffield
PMCID: PMC1801487  PMID: 7573061

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Buetow K. H., Weber J. L., Ludwigsen S., Scherpbier-Heddema T., Duyk G. M., Sheffield V. C., Wang Z., Murray J. C. Integrated human genome-wide maps constructed using the CEPH reference panel. Nat Genet. 1994 Apr;6(4):391–393. doi: 10.1038/ng0494-391. [DOI] [PubMed] [Google Scholar]
  2. Chaïb H., Lina-Granade G., Guilford P., Plauchu H., Levilliers J., Morgon A., Petit C. A gene responsible for a dominant form of neurosensory non-syndromic deafness maps to the NSRD1 recessive deafness gene interval. Hum Mol Genet. 1994 Dec;3(12):2219–2222. doi: 10.1093/hmg/3.12.2219. [DOI] [PubMed] [Google Scholar]
  3. Chen A. H., Ni L., Fukushima K., Marietta J., O'Neill M., Coucke P., Willems P., Smith R. J. Linkage of a gene for dominant non-syndromic deafness to chromosome 19. Hum Mol Genet. 1995 Jun;4(6):1073–1076. doi: 10.1093/hmg/4.6.1073. [DOI] [PubMed] [Google Scholar]
  4. Coucke P., Van Camp G., Djoyodiharjo B., Smith S. D., Frants R. R., Padberg G. W., Darby J. K., Huizing E. H., Cremers C. W., Kimberling W. J. Linkage of autosomal dominant hearing loss to the short arm of chromosome 1 in two families. N Engl J Med. 1994 Aug 18;331(7):425–431. doi: 10.1056/NEJM199408183310702. [DOI] [PubMed] [Google Scholar]
  5. Friedman T. B., Liang Y., Weber J. L., Hinnant J. T., Barber T. D., Winata S., Arhya I. N., Asher J. H., Jr A gene for congenital, recessive deafness DFNB3 maps to the pericentromeric region of chromosome 17. Nat Genet. 1995 Jan;9(1):86–91. doi: 10.1038/ng0195-86. [DOI] [PubMed] [Google Scholar]
  6. Guilford P., Ayadi H., Blanchard S., Chaib H., Le Paslier D., Weissenbach J., Drira M., Petit C. A human gene responsible for neurosensory, non-syndromic recessive deafness is a candidate homologue of the mouse sh-1 gene. Hum Mol Genet. 1994 Jun;3(6):989–993. doi: 10.1093/hmg/3.6.989. [DOI] [PubMed] [Google Scholar]
  7. Guilford P., Ben Arab S., Blanchard S., Levilliers J., Weissenbach J., Belkahia A., Petit C. A non-syndrome form of neurosensory, recessive deafness maps to the pericentromeric region of chromosome 13q. Nat Genet. 1994 Jan;6(1):24–28. doi: 10.1038/ng0194-24. [DOI] [PubMed] [Google Scholar]
  8. Leon P. E., Raventos H., Lynch E., Morrow J., King M. C. The gene for an inherited form of deafness maps to chromosome 5q31. Proc Natl Acad Sci U S A. 1992 Jun 1;89(11):5181–5184. doi: 10.1073/pnas.89.11.5181. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Moatti L., Garabedian E. N., Lacombe H., Spir-Jacob C. Surdités de perception congénitales et syndromes associés. Ann Otolaryngol Chir Cervicofac. 1990;107(3):181–186. [PubMed] [Google Scholar]
  10. Petrukhin K. E., Speer M. C., Cayanis E., Bonaldo M. F., Tantravahi U., Soares M. B., Fischer S. G., Warburton D., Gilliam T. C., Ott J. A microsatellite genetic linkage map of human chromosome 13. Genomics. 1993 Jan;15(1):76–85. doi: 10.1006/geno.1993.1012. [DOI] [PubMed] [Google Scholar]
  11. Reardon W., Roberts S., Phelps P. D., Thomas N. S., Beck L., Issac R., Hughes H. E. Phenotypic evidence for a common pathogenesis in X-linked deafness pedigrees and in Xq13-q21 deletion related deafness. Am J Med Genet. 1992 Nov 1;44(4):513–517. doi: 10.1002/ajmg.1320440427. [DOI] [PubMed] [Google Scholar]
  12. Robinson D., Lamont M., Curtis G., Shields D. C., Phelps P. A family with X-linked deafness showing linkage to the proximal Xq region of the X chromosome. Hum Genet. 1992 Nov;90(3):316–318. doi: 10.1007/BF00220090. [DOI] [PubMed] [Google Scholar]

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