These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

193 related articles for article (PubMed ID: 1407588)

  • 1. Analysis of the DNA duplication 17p11.2 in Charcot-Marie-Tooth neuropathy type 1 pedigrees: additional evidence for a third autosomal CMT1 locus.
    Chance PF; Matsunami N; Lensch W; Smith B; Bird TD
    Neurology; 1992 Oct; 42(10):2037-41. PubMed ID: 1407588
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Estimation of the size of the chromosome 17p11.2 duplication in Charcot-Marie-Tooth neuropathy type 1a (CMT1a). HMSN Collaborative Research Group.
    Raeymaekers P; Timmerman V; Nelis E; Van Hul W; De Jonghe P; Martin JJ; Van Broeckhoven C
    J Med Genet; 1992 Jan; 29(1):5-11. PubMed ID: 1552545
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Charcot-Marie-Tooth disease in northern Sweden: pedigree analysis and the presence of the duplication in chromosome 17p11.2.
    Holmberg BH; Holmgren G; Nelis E; van Broeckhoven C; Westerberg B
    J Med Genet; 1994 Jun; 31(6):435-41. PubMed ID: 8071969
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Duplication within chromosome 17p11.2 in 12 families of French ancestry with Charcot-Marie-Tooth disease type 1a. The French CMT Research Group.
    Brice A; Ravisé N; Stevanin G; Gugenheim M; Bouche P; Penet C; Agid Y
    J Med Genet; 1992 Nov; 29(11):807-12. PubMed ID: 1453432
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Clinical and genetic heterogeneity of Charcot-Marie-Tooth disease.
    Hentati A; Lamy C; Melki J; Zuber M; Munnich A; de Recondo J
    Genomics; 1992 Jan; 12(1):155-7. PubMed ID: 1733853
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Genetic evaluation of inherited motor/sensory neuropathy.
    Chance PF
    Suppl Clin Neurophysiol; 2004; 57():228-42. PubMed ID: 16106622
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Duplication of part of chromosome 17 is commonly associated with hereditary motor and sensory neuropathy type I (Charcot-Marie-Tooth disease type 1).
    Hallam PJ; Harding AE; Berciano J; Barker DF; Malcolm S
    Ann Neurol; 1992 May; 31(5):570-2. PubMed ID: 1596093
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [The diagnosis and prevalence of locus CMT1A duplication in Charcot-Marie-Tooth disease type 1].
    Bort S; Sevilla T; Vílchez JJ; Prieto F; Palau F
    Med Clin (Barc); 1995 May; 104(17):648-52. PubMed ID: 7623491
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. 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]  

  • 11. [Analysis of mutations in the chromosome 17p11.2 region in patients with Charcot-Marie-Tooth type 1 disease and in patients with tomaculous neuropathy].
    Zamurović N; Milić V; Dacković J; Zamurović D; Culjković B; Parlović S; Apostolski S; Romac S
    Srp Arh Celok Lek; 2002; 130(3-4):59-63. PubMed ID: 12154515
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Study of the duplication of 17p11.2-12 chromosome region in the patients with hereditary motor and sensory neuropathy type 1A].
    Hryshchenko NV; Bychkova AM; Pichkur NA; Skyban HV; Dmytrenko VV; Livshyts' LA
    Tsitol Genet; 2003; 37(6):55-9. PubMed ID: 15067947
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Allelic heterogeneity in hereditary motor and sensory neuropathy type Ia (Charcot-Marie-Tooth disease type 1a).
    Hoogendijk JE; Janssen EA; Gabreëls-Festen AA; Hensels GW; Joosten EM; Gabreëls FJ; Zorn I; Valentijn LJ; Baas F; Ongerboer de Visser BW
    Neurology; 1993 May; 43(5):1010-5. PubMed ID: 8492918
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Molecular genetics and neuropathology of Charcot-Marie-Tooth disease type 1A.
    Lupski JR; Garcia CA
    Brain Pathol; 1992 Oct; 2(4):337-49. PubMed ID: 1341967
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Charcot-Marie-Tooth disease: molecular characterization of patients from central and southern Italy.
    Guzzetta V; Santoro L; Gasparo-Rippa P; Ragno M; Vita G; Caruso G; Andria G
    Clin Genet; 1995 Jan; 47(1):27-32. PubMed ID: 7774040
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Linkage and mutation analysis in an extended family with Charcot-Marie-Tooth disease type 1B.
    Nelis E; Timmerman V; De Jonghe P; Muylle L; Martin JJ; Van Broeckhoven C
    J Med Genet; 1994 Oct; 31(10):811-5. PubMed ID: 7530774
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The peripheral myelin protein gene PMP-22 is contained within the Charcot-Marie-Tooth disease type 1A duplication.
    Timmerman V; Nelis E; Van Hul W; Nieuwenhuijsen BW; Chen KL; Wang S; Ben Othman K; Cullen B; Leach RJ; Hanemann CO
    Nat Genet; 1992 Jun; 1(3):171-5. PubMed ID: 1303230
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Prenatal diagnosis of Charcot-Marie-Tooth disease type 1A by multicolor in situ hybridization.
    Lebo RV; Martelli L; Su Y; Li L; Lynch E; Mansfield E; Pua KH; Watson DF; Chueh J; Hurko O
    Am J Med Genet; 1993 Sep; 47(3):441-50. PubMed ID: 8135298
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A novel type of hereditary motor and sensory neuropathy characterized by a mild phenotype.
    De Jonghe P; Timmerman V; Nelis E; De Vriendt E; Löfgren A; Ceuterick C; Martin JJ; Van Broeckhoven C
    Arch Neurol; 1999 Oct; 56(10):1283-8. PubMed ID: 10520946
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Chromosome I linkage studies in Charcot-Marie-Tooth neuropathy type I.
    Griffiths LR; Zwi MB; McLeod JG; Nicholson GA
    Am J Hum Genet; 1988 May; 42(5):756-71. PubMed ID: 2895983
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.