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Volumn 34, Issue 1, 1996, Pages 128-133

A 1.5-Mb cosmid contig of the CMT1A duplication/HNPP deletion critical region in 17p11.2-p12

Author keywords

[No Author keywords available]

Indexed keywords

DNA FRAGMENT; GENE PRODUCT; MYELIN PROTEIN;

EID: 0030066532     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.1996.0251     Document Type: Article
Times cited : (12)

References (20)
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  • 3
    • 0027512552 scopus 로고
    • Charcot-Marie-Tooth neuropathy type IA with both duplication and non-duplication
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    • Ionasescu, V.V.1    Ionasescu, R.2    Searby, C.3    Barker, D.F.4
  • 4
    • 0028201453 scopus 로고
    • Physical mapping of chromosome 17 cosmids by fluorescence in situ hybridization and digital image analysis
    • Kallioniemi, O.-P., Kallioniemi, A., Mascio, L., Sudar, D., Pinkel, D., Deaven, L., and Gray, J. (1994). Physical mapping of chromosome 17 cosmids by fluorescence in situ hybridization and digital image analysis. Genomics 20: 125-128.
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  • 5
    • 0028810444 scopus 로고
    • Analysis of the CMT1A-REP repeat: Mapping crossover breakpoints in CMT1A and HNPP
    • Kiyosawa, H., Lensch, M. W., and Chance, P. F. (1995). Analysis of the CMT1A-REP repeat: Mapping crossover breakpoints in CMT1A and HNPP. Hum. Mol. Genet. 4: 2327-2334.
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    • Kiyosawa, H.1    Lensch, M.W.2    Chance, P.F.3
  • 7
    • 0027366552 scopus 로고
    • Inherited primary peripheral neuropathies: Molecular genetics and clinical implications of CMT1A and HNPP
    • Lupski, J. R., Chance, P. F., and Garcia, C. A. (1993). Inherited primary peripheral neuropathies: Molecular genetics and clinical implications of CMT1A and HNPP. J. Am. Med. Assoc. 270: 2326-2330.
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    • Lupski, J.R.1    Chance, P.F.2    Garcia, C.A.3
  • 8
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    • Nelis, E., Van Broeckhoven, C., et al. (1996). Estimation of the mutation frequencies in Charcot-Marie-Tooth disease type 1 (CMT1) and hereditary neuropathy with liability to pressure palsies (HNPP): A European collaborative study. Eur. J. Hum. Genet. 4: 25-33.
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    • Patil, N., Peterson, A., Rothman, A., de Jong, P. J., Myers, R. M., and Cox, D. R. (1994). A high resolution physical map of 2.5 Mbp of the Down syndrome region on chromosome 21. Hum. Mol. Genet. 3: 1811-1817.
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  • 19
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.