BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

199 related articles for article (PubMed ID: 14606043)

  • 1. Dominant intermediate Charcot-Marie-Tooth type C maps to chromosome 1p34-p35.
    Jordanova A; Thomas FP; Guergueltcheva V; Tournev I; Gondim FA; Ishpekova B; De Vriendt E; Jacobs A; Litvinenko I; Ivanova N; Buzhov B; De Jonghe P; Kremensky I; Timmerman V
    Am J Hum Genet; 2003 Dec; 73(6):1423-30. PubMed ID: 14606043
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Dominant intermediate Charcot-Marie-Tooth neuropathy maps to chromosome 19p12-p13.2.
    Kennerson ML; Zhu D; Gardner RJ; Storey E; Merory J; Robertson SP; Nicholson GA
    Am J Hum Genet; 2001 Oct; 69(4):883-8. PubMed ID: 11533912
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Refined localization of dominant intermediate Charcot-Marie-Tooth neuropathy and exclusion of seven known candidate genes in the region.
    Zhu D; Kennerson M; Merory J; Chrast R; Verheijen M; Lemke G; Nicholson G
    Neurogenetics; 2003 Aug; 4(4):179-83. PubMed ID: 12761657
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A locus for an axonal form of autosomal recessive Charcot-Marie-Tooth disease maps to chromosome 1q21.2-q21.3.
    Bouhouche A; Benomar A; Birouk N; Mularoni A; Meggouh F; Tassin J; Grid D; Vandenberghe A; Yahyaoui M; Chkili T; Brice A; LeGuern E
    Am J Hum Genet; 1999 Sep; 65(3):722-7. PubMed ID: 10441578
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Localization of the gene for the intermediate form of Charcot-Marie-Tooth to chromosome 10q24.1-q25.1.
    Verhoeven K; Villanova M; Rossi A; Malandrini A; De Jonghe P; Timmerman V
    Am J Hum Genet; 2001 Oct; 69(4):889-94. PubMed ID: 11533914
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mapping of Charcot-Marie-Tooth disease type 1C to chromosome 16p identifies a novel locus for demyelinating neuropathies.
    Street VA; Goldy JD; Golden AS; Tempel BL; Bird TD; Chance PF
    Am J Hum Genet; 2002 Jan; 70(1):244-50. PubMed ID: 11713717
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A new locus for autosomal dominant Charcot-Marie-Tooth disease type 2 (CMT2L) maps to chromosome 12q24.
    Tang BS; Luo W; Xia K; Xiao JF; Jiang H; Shen L; Tang JG; Zhao GH; Cai F; Pan Q; Dai HP; Yang QD; Xia JH; Evgrafov OV
    Hum Genet; 2004 May; 114(6):527-33. PubMed ID: 15021985
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genetic epidemiology of Charcot-Marie-Tooth disease.
    Braathen GJ
    Acta Neurol Scand Suppl; 2012; (193):iv-22. PubMed ID: 23106488
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Study on the gene and phenotypic characterisation of autosomal recessive demyelinating motor and sensory neuropathy (Charcot-Marie-Tooth disease) with a gene locus on chromosome 5q23-q33.
    Gabreëls-Festen A; van Beersum S; Eshuis L; LeGuern E; Gabreëls F; van Engelen B; Mariman E
    J Neurol Neurosurg Psychiatry; 1999 May; 66(5):569-74. PubMed ID: 10209165
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genetic linkage and heterogeneity in type I Charcot-Marie-Tooth disease (hereditary motor and sensory neuropathy type I).
    Chance PF; Bird TD; O'Connell P; Lipe H; Lalouel JM; Leppert M
    Am J Hum Genet; 1990 Dec; 47(6):915-25. PubMed ID: 2239969
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Homozygosity mapping of an autosomal recessive form of demyelinating Charcot-Marie-Tooth disease to chromosome 5q23-q33.
    LeGuern E; Guilbot A; Kessali M; Ravisé N; Tassin J; Maisonobe T; Grid D; Brice A
    Hum Mol Genet; 1996 Oct; 5(10):1685-8. PubMed ID: 8894708
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Heterogeneity in X-linked recessive Charcot-Marie-Tooth neuropathy.
    Ionasescu VV; Trofatter J; Haines JL; Summers AM; Ionasescu R; Searby C
    Am J Hum Genet; 1991 Jun; 48(6):1075-83. PubMed ID: 1674639
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Charcot-Marie-Tooth neuropathy related to chromosome 1.
    Ionasescu VV; Trofatter J; Haines JL; Ionasescu R; Searby C
    Am J Med Genet; 1992 Mar; 42(5):728-32. PubMed ID: 1632448
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Localization of a gene (CMT2A) for autosomal dominant Charcot-Marie-Tooth disease type 2 to chromosome 1p and evidence of genetic heterogeneity.
    Ben Othmane K; Middleton LT; Loprest LJ; Wilkinson KM; Lennon F; Rozear MP; Stajich JM; Gaskell PC; Roses AD; Pericak-Vance MA
    Genomics; 1993 Aug; 17(2):370-5. PubMed ID: 8406488
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Localization of the mutation in an extended family with Charcot-Marie-Tooth neuropathy (HMSN I).
    Raeymaekers P; Timmerman V; De Jonghe P; Swerts L; Gheuens J; Martin JJ; Muylle L; De Winter G; Vandenberghe A; Van Broeckhoven C
    Am J Hum Genet; 1989 Dec; 45(6):953-8. PubMed ID: 2589322
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Localization of a locus for Charcot-Marie-Tooth neuropathy type Ia (CMT1A) to chromosome 17.
    McAlpine PJ; Feasby TE; Hahn AF; Komarnicki L; James S; Guy C; Dixon M; Qayyum S; Wright J; Coopland G
    Genomics; 1990 Jul; 7(3):408-15. PubMed ID: 2365358
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Proof of genetic heterogeneity in X-linked Charcot-Marie-Tooth disease.
    Huttner IG; Kennerson ML; Reddel SW; Radovanovic D; Nicholson GA
    Neurology; 2006 Dec; 67(11):2016-21. PubMed ID: 17159110
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Assignment of a second Charcot-Marie-Tooth type II locus to chromosome 3q.
    Kwon JM; Elliott JL; Yee WC; Ivanovich J; Scavarda NJ; Moolsintong PJ; Goodfellow PJ
    Am J Hum Genet; 1995 Oct; 57(4):853-8. PubMed ID: 7573046
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.