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Journal Abstract Search

201 related items for PubMed ID: 2987105

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  • 2. Localization of X-linked dominant Charcot-Marie-Tooth disease (CMT 2) to Xq13.
    Beckett J, Holden JJ, Simpson NE, White BN, MacLeod PM.
    J Neurogenet; 1986 Jul; 3(4):225-31. PubMed ID: 3462379
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  • 3. A linkage study of the locus for X-linked Charcot-Marie-Tooth disease.
    Goonewardena P, Welihinda J, Anvret M, Gyftodimou J, Haegermark A, Iselius L, Lindsten J, Pettersson U.
    Clin Genet; 1988 Jun; 33(6):435-40. PubMed ID: 2901924
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  • 4. Mapping of the gene for X-linked dominant Charcot-Marie-Tooth neuropathy.
    Ionasescu VV, Trofatter J, Haines JL, Ionasescu R, Searby C.
    Neurology; 1992 Apr; 42(4):903-8. PubMed ID: 1565250
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  • 8. X-linked Charcot-Marie-Tooth disease. A linkage study in a large family by using 12 probes of the pericentromeric region.
    Mostacciuolo ML, Müller E, Fardin P, Micaglio GF, Bardoni B, Guioli S, Camerino G, Danieli GA.
    Hum Genet; 1991 May; 87(1):23-7. PubMed ID: 1674715
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  • 9. Genetic linkage relationships of Charcot-Marie-Tooth disease (HMSN-Ib) to chromosome 1 markers.
    Chance PF, Murray JC, Bird TD, Kochin RS.
    Neurology; 1987 Feb; 37(2):325-9. PubMed ID: 3468376
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  • 11. X linked Charcot-Marie-Tooth disease (CMTX1): a study of 15 families with 12 highly informative polymorphisms.
    Cochrane S, Bergoffen J, Fairweather ND, Müller E, Mostacciuolo ML, Monaco AP, Fischbeck KH, Haites NE.
    J Med Genet; 1994 Mar; 31(3):193-6. PubMed ID: 7912286
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  • 12. Genetic mapping of autosomal dominant Charcot-Marie-Tooth disease in a large French-Acadian kindred: identification of new linked markers on chromosome 17.
    Patel PI, Franco B, Garcia C, Slaugenhaupt SA, Nakamura Y, Ledbetter DH, Chakravarti A, Lupski JR.
    Am J Hum Genet; 1990 Apr; 46(4):801-9. PubMed ID: 2316525
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  • 13. X-linked mixed deafness with stapes fixation in a Mauritian kindred: linkage to Xq probe pDP34.
    Wallis C, Ballo R, Wallis G, Beighton P, Goldblatt J.
    Genomics; 1988 Nov; 3(4):299-301. PubMed ID: 3243543
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  • 16. Linkage localization of X-linked Charcot-Marie-Tooth disease.
    Bergoffen J, Trofatter J, Pericak-Vance MA, Haines JL, Chance PF, Fischbeck KH.
    Am J Hum Genet; 1993 Feb; 52(2):312-8. PubMed ID: 8430694
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  • 18. Choroideremia is linked to the restriction fragment length polymorphism DXYS1 at XQ13-21.
    Nussbaum RL, Lewis RA, Lesko JG, Ferrell R.
    Am J Hum Genet; 1985 May; 37(3):473-81. PubMed ID: 2988333
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  • 19. Evidence for linkage of Charcot-Marie-Tooth neuropathy to the Duffy locus on chromosome 1.
    Bird TD, Ott J, Giblett ER.
    Am J Hum Genet; 1982 May; 34(3):388-94. PubMed ID: 6952764
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