BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

118 related articles for article (PubMed ID: 3319438)

  • 1. Regional chromosomal assignment of human renin gene to 1q12----qter and use in linkage studies in Charcot-Marie-Tooth disease.
    Griffiths LR; Nicholson GA; Ross DA; Zwi MB; McLeod JG; Mohandas T; Morris BJ
    Cytogenet Cell Genet; 1987; 45(3-4):231-3. PubMed ID: 3319438
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Isolation and use of chromosome 1 probes for linkage studies on Charcot-Marie-Tooth disease.
    Griffiths LR; Zwi MB; Mesterovic N; Ross DA; Board PG; Callen DF; Mohandas T; Buckland R; Fletcher JM; Driesel AJ
    Ann Hum Genet; 1990 Jan; 54(1):31-7. PubMed ID: 2321912
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Evidence for linkage of Charcot-Marie-Tooth neuropathy (CMT1) to apolipoprotein A2 (Apo-A2).
    Ionasescu V; Anderson R; Burns TL; Searby C; Ionasescu R; Ferrell R
    Am J Hum Genet; 1988 Jan; 42(1):74-6. PubMed ID: 3122561
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Absence of genetic linkage of Charcot-Marie-Tooth disease (HMSN Ia) with chromosome 1 gene markers.
    Raeymaekers P; De Jonghe P; Backhovens H; Wehnert A; De Winter G; Swerts L; Gheuens J; Martin JJ; Vandenberghe A; Van Broeckhoven C
    Neurology; 1989 Jun; 39(6):844-6. PubMed ID: 2725880
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Linkage analysis of the Duffy blood group marker with several chromosome 1 genes in an extended pedigree with Charcot-Marie-Tooth disease.
    Raeymaekers P; Van Broeckhoven C; Backhovens H; Wehnert A; Muylle L; De Jonghe P; Gheuens J; Martin JJ; Vandenberghe A
    Hum Genet; 1989 Feb; 81(3):231-3. PubMed ID: 2921030
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Linkage between the loci for autosomal dominant neuronal Charcot-Marie-Tooth neuropathy (CMT1) and serum amyloid P component (APCS) on human chromosome 1.
    Ionasescu V; Burns T; Searby C; Ionasescu R; Whitehead AS
    Cytogenet Cell Genet; 1988; 47(3):175-6. PubMed ID: 3163970
    [No Abstract]   [Full Text] [Related]  

  • 9. Linkage in a family with X-linked Charcot-Marie-Tooth disease.
    Haites N; Fairweather N; Clark C; Kelly KF; Simpson S; Johnston AW
    Clin Genet; 1989 Jun; 35(6):399-403. PubMed ID: 2567643
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Genetic linkage of the autosomal dominant form of Charcot-Marie-Tooth amyotrophy and 3 genetic markers on chromosome 1].
    Ferák V; Kádasi L; Hrubisko M; Siváková D; Véghová E
    Cesk Neurol Neurochir; 1989 May; 52(3):200-7. PubMed ID: 2582521
    [TBL] [Abstract][Full Text] [Related]  

  • 11. DNA probes in Charcot-Marie-Tooth neuropathy.
    Nicholson GA; Griffiths LR; McLeod JG
    Aust Paediatr J; 1988; 24 Suppl 1():90-1. PubMed ID: 3202739
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Genetic linkage of hereditary motor and sensory neuropathy type I (Charcot-Marie-Tooth disease) to markers of chromosomes 1 and 17.
    Defesche JC; Hoogendijk JE; de Visser M; de Visser O; Bolhuis PA
    Neurology; 1990 Sep; 40(9):1450-3. PubMed ID: 2392234
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Exclusion analysis of Charcot-Marie-Tooth neuropathy (CMT1) with chromosome 1p markers.
    Raeymaekers P; De Jonghe P; Swerts L; De Winter G; Gheuens J; Martin JJ; Vandenberghe A; Van Broeckhoven C
    Cytogenet Cell Genet; 1989; 50(2-3):178-80. PubMed ID: 2570676
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Heterogeneity evidence and linkage studies on Charcot-Marie-Tooth disease.
    Griffiths LR; Zwi MB; McLeod JG; Ross DA; Nicholson GA
    Neurology; 1989 Feb; 39(2 Pt 1):280-1. PubMed ID: 2915802
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The Duffy blood group is linked to the alpha-spectrin locus in a large pedigree with autosomal dominant inheritance of Charcot-Marie-Tooth disease type 1.
    Raeymaekers P; Van Broeckhoven C; Backhovens H; Wehnert A; Muylle L; De Jonghe P; Gheuens J; Vandenberghe A
    Hum Genet; 1988 Jan; 78(1):76-8. PubMed ID: 2892777
    [TBL] [Abstract][Full Text] [Related]  

  • 18. X-linked dominant Charcot-Marie-Tooth disease: suggestion of linkage with a cloned DNA sequence from the proximal Xq.
    Gal A; Mücke J; Theile H; Wieacker PF; Ropers HH; Wienker TF
    Hum Genet; 1985; 70(1):38-42. PubMed ID: 2987105
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Autosomal dominant distal spinal muscular atrophy type V (dSMA-V) and Charcot-Marie-Tooth disease type 2D (CMT2D) segregate within a single large kindred and map to a refined region on chromosome 7p15.
    Sambuughin N; Sivakumar K; Selenge B; Lee HS; Friedlich D; Baasanjav D; Dalakas MC; Goldfarb LG
    J Neurol Sci; 1998 Nov; 161(1):23-8. PubMed ID: 9879677
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Linkage of Charcot-Marie-Tooth neuropathy type 1a to chromosome 17.
    Vance JM; Nicholson GA; Yamaoka LH; Stajich J; Stewart CS; Speer MC; Hung WY; Roses AD; Barker D; Pericak-Vance MA
    Exp Neurol; 1989 May; 104(2):186-9. PubMed ID: 2707366
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.