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American Journal of Human Genetics
Volumn 59, Issue 2, 1996, Pages 385-391
An autosomal recessive nonsyndromic-hearing-loss locus identified by DNA pooling using two inbred bedouin kindreds
Author keywords

[No Author keywords available]
Indexed keywords

DNA;
EID: 0029811339     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (65)
References (6)
  • 1
    • 0029145428 scopus 로고
    • Linkage of congenital, recessive deafness (DFNB4) to chromosome 7q31 and evidence for genetic heterogeneity in the Middle Eastern Druze population
    • Baldwin CT, Weiss S, Farrer LA, DeStefano AL, Adair R, Franklyn B, Bonne-Tamir B, et al (1995) Linkage of congenital, recessive deafness (DFNB4) to chromosome 7q31 and evidence for genetic heterogeneity in the Middle Eastern Druze population. Hum Mol Genet 4:1637-1642
    • (1995) Hum Mol Genet , vol.4 , pp. 1637-1642
    • Baldwin, C.T.1    Weiss, S.2    Farrer, L.A.3    DeStefano, A.L.4    Adair, R.5    Franklyn, B.6    Bonne-Tamir, B.7
  • 2
    • 0025835296 scopus 로고
    • Fast and sensitive silver staining of DNA in polyacrylamide gels
    • Bassam BJ, Caetano-Anolles G, Gressholff PM (1991) Fast and sensitive silver staining of DNA in polyacrylamide gels. Anal Biochem 196:80-83
    • (1991) Anal Biochem , vol.196 , pp. 80-83
    • Bassam, B.J.1    Caetano-Anolles, G.2    Gressholff, P.M.3
  • 3
    • 0027483310 scopus 로고
    • A form of sensori-neural deafness is determined by a mitochondrial and an autosomal locus: Evidence from pedigree segregation analysis
    • Bu X, Shohart M, Jaber L, Rotter JI (1993) A form of sensori-neural deafness is determined by a mitochondrial and an autosomal locus: evidence from pedigree segregation analysis Genet Epidemiol 10:3-15
    • (1993) Genet Epidemiol , vol.10 , pp. 3-15
    • Bu, X.1    Shohart, M.2    Jaber, L.3    Rotter, J.I.4
  • 5
    • 0028555358 scopus 로고
    • A gene responsible for a dominant form of neurosensory nonsyndromic deafness maps to the NSRD1 recessive deafness gene interval
    • Chaib H, Lina-Granade G, Guilford P, Plaucho H, Levillier J, Morgon A, Petit C (1994) A gene responsible for a dominant form of neurosensory nonsyndromic deafness maps to the NSRD1 recessive deafness gene interval. Hum Mol Genet 3:2219-2222
    • (1994) Hum Mol Genet , vol.3 , pp. 2219-2222
    • Chaib, H.1    Lina-Granade, G.2    Guilford, P.3    Plaucho, H.4    Levillier, J.5    Morgon, A.6    Petit, C.7
  • 6
    • 0030047197 scopus 로고    scopus 로고
    • A gene responsible for a sensorineural nonsyndromic recessive deafness maps to chromosome 2p22-23
    • Chaib H, Place C, Salem N, Chardenoux S, Vincent C, Weissenbach J, Petit C, et al (1996) A gene responsible for a sensorineural nonsyndromic recessive deafness maps to chromosome 2p22-23. Hum Mol Genet 5:155-158
    • (1996) Hum Mol Genet , vol.5 , pp. 155-158
    • Chaib, H.1    Place, C.2    Salem, N.3    Chardenoux, S.4    Vincent, C.5    Weissenbach, J.6    Petit, C.7

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.