BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

141 related articles for article (PubMed ID: 2688822)

  • 21. Molecular deletion patterns in Duchenne muscular dystrophy patients.
    Lucotte G; David F; Levy C
    Ann Genet; 1989; 32(4):214-9. PubMed ID: 2610487
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [Molecular pathology of Duchenne and Becker muscular dystrophy].
    Gilgenkrantz H; Chelly J; Récan D; Chafey P; Kaplan JC
    C R Seances Soc Biol Fil; 1992; 186(4):349-53. PubMed ID: 1301222
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [Molecular genetics and problems found in genetic diagnosis of Duchenne Becker muscular dystrophy].
    Takeshima Y; Matsuo M
    Nihon Rinsho; 1997 Dec; 55(12):3120-5. PubMed ID: 9436421
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [Deletions within the gene of dystrophin in Duchenne and Becker muscular dystrophy].
    Zimowski JG; Bisko M; Fidziańska E; Hausmanowa-Petrusewicz I; Badurska B; Borkowska J; Lusakowska A; Fidziańska A; Jezuita J; Zaremba J
    Neurol Neurochir Pol; 1993; 27(4):469-78. PubMed ID: 8247234
    [TBL] [Abstract][Full Text] [Related]  

  • 25. The Wellcome lecture, 1988. Muscular dystrophy: a time of hope.
    Kunkel LM
    Proc R Soc Lond B Biol Sci; 1989 Jun; 237(1286):1-9. PubMed ID: 2569197
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Preferential deletion of exons in Duchenne and Becker muscular dystrophies.
    Forrest SM; Cross GS; Speer A; Gardner-Medwin D; Burn J; Davies KE
    Nature; 1987 Oct 15-21; 329(6140):638-40. PubMed ID: 2821406
    [TBL] [Abstract][Full Text] [Related]  

  • 27. An explanation for the phenotypic differences between patients bearing partial deletions of the DMD locus.
    Monaco AP; Bertelson CJ; Liechti-Gallati S; Moser H; Kunkel LM
    Genomics; 1988 Jan; 2(1):90-5. PubMed ID: 3384440
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Molecular deletion patterns in Duchenne and Becker type muscular dystrophy.
    Liechti-Gallati S; Koenig M; Kunkel LM; Frey D; Boltshauser E; Schneider V; Braga S; Moser H
    Hum Genet; 1989 Mar; 81(4):343-8. PubMed ID: 2784778
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Transcription of the dystrophin gene in Duchenne muscular dystrophy muscle.
    Muntoni F; Strong PN
    FEBS Lett; 1989 Jul; 252(1-2):95-8. PubMed ID: 2668030
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Genotype-phenotype correlation in Duchenne/Becker muscular dystrophy patients seen at Lucknow.
    Mittal B; Singh V; Mishra S; Sinha S; Mittal RD; Chaturvedi LS; Danda S; Pradhan S; Agarwal SS
    Indian J Med Res; 1997 Jan; 105():32-8. PubMed ID: 9029833
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Topography of the Duchenne muscular dystrophy (DMD) gene: FIGE and cDNA analysis of 194 cases reveals 115 deletions and 13 duplications.
    Den Dunnen JT; Grootscholten PM; Bakker E; Blonden LA; Ginjaar HB; Wapenaar MC; van Paassen HM; van Broeckhoven C; Pearson PL; van Ommen GJ
    Am J Hum Genet; 1989 Dec; 45(6):835-47. PubMed ID: 2573997
    [TBL] [Abstract][Full Text] [Related]  

  • 32. High resolution deletion breakpoint mapping in the DMD gene by whole cosmid hybridization.
    Blonden LA; den Dunnen JT; van Paassen HM; Wapenaar MC; Grootscholten PM; Ginjaar HB; Bakker E; Pearson PL; van Ommen GJ
    Nucleic Acids Res; 1989 Jul; 17(14):5611-21. PubMed ID: 2569720
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Relatively low proportion of dystrophin gene deletions in Israeli Duchenne and Becker muscular dystrophy patients.
    Shomrat R; Gluck E; Legum C; Shiloh Y
    Am J Med Genet; 1994 Feb; 49(4):369-73. PubMed ID: 8160727
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Dystrophin as a diagnostic marker in Duchenne and Becker muscular dystrophy. Correlation of immunofluorescence and western blot.
    Voit T; Stuettgen P; Cremer M; Goebel HH
    Neuropediatrics; 1991 Aug; 22(3):152-62. PubMed ID: 1944822
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Molecular and clinical correlations of deletions leading to Duchenne and Becker muscular dystrophies.
    Baumbach LL; Chamberlain JS; Ward PA; Farwell NJ; Caskey CT
    Neurology; 1989 Apr; 39(4):465-74. PubMed ID: 2927671
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [Molecular genetics of Duchenne/Becker muscular dystrophy].
    Saito K; Ikeya K; Kondo E; Yamauchi A; Komine S; Fukuyama Y
    Nihon Rinsho; 1993 Sep; 51(9):2420-7. PubMed ID: 8411723
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Mild and severe muscular dystrophy associated with deletions in Xp21 of the human X chromosome.
    Davies KE; Smith TJ; Bundey S; Read AP; Flint T; Bell M; Speer A
    J Med Genet; 1988 Jan; 25(1):9-13. PubMed ID: 3162536
    [TBL] [Abstract][Full Text] [Related]  

  • 38. DNA deletions in mild and severe Becker muscular dystrophy.
    Hart KA; Hodgson S; Walker A; Cole CG; Johnson L; Dubowitz V; Bobrow M
    Hum Genet; 1987 Mar; 75(3):281-5. PubMed ID: 3030926
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Dystrophin-related muscular dystrophies.
    Witkowski JA
    J Child Neurol; 1989 Oct; 4(4):251-71. PubMed ID: 2571631
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Gene deletions in Japanese patients with Duchenne and Becker muscular dystrophy.
    Asano J; Tomatsu S; Sukegawa K; Yamaguchi S; Ikedo Y; Minami R; Iida M; Nishimura M; Nakagawa M; Ohshiro M
    Jinrui Idengaku Zasshi; 1990 Jun; 35(2):159-68. PubMed ID: 2398631
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.