BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

207 related articles for article (PubMed ID: 3410474)

  • 1. Further studies of gene deletions that cause Duchenne and Becker muscular dystrophies.
    Forrest SM; Cross GS; Flint T; Speer A; Robson KJ; Davies KE
    Genomics; 1988 Feb; 2(2):109-14. PubMed ID: 3410474
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Duchenne and Becker muscular dystrophy mutations: analysis using 2.6 kb of muscle cDNA from the 5' end of the gene.
    Smith TJ; Forrest SM; Cross GS; Davies KE
    Nucleic Acids Res; 1987 Dec; 15(23):9761-9. PubMed ID: 3697082
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Patterns of exon deletions in Duchenne and Becker muscular dystrophy.
    Read AP; Mountford RC; Forrest SM; Kenwrick SJ; Davies KE; Harris R
    Hum Genet; 1988 Oct; 80(2):152-6. PubMed ID: 3169738
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 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]  

  • 6. A deletion hot spot in the Duchenne muscular dystrophy gene.
    Wapenaar MC; Kievits T; Hart KA; Abbs S; Blonden LA; den Dunnen JT; Grootscholten PM; Bakker E; Verellen-Dumoulin C; Bobrow M
    Genomics; 1988 Feb; 2(2):101-8. PubMed ID: 2900805
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Molecular deletions in the Duchenne/Becker muscular dystrophy gene.
    Hart KA; Abbs S; Wapenaar MC; Cole CG; Hodgson SV; Bobrow M
    Clin Genet; 1989 Apr; 35(4):251-60. PubMed ID: 2653672
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The molecular basis for Duchenne versus Becker muscular dystrophy: correlation of severity with type of deletion.
    Koenig M; Beggs AH; Moyer M; Scherpf S; Heindrich K; Bettecken T; Meng G; Müller CR; Lindlöf M; Kaariainen H; de la Chapellet A; Kiuru A; Savontaus ML; Gilgenkrantz H; Récan D; Chelly J; Kaplan JC; Covone AE; Archidiacono N; Romeo G; Liechti-Gailati S; Schneider V; Braga S; Moser H; Darras BT; Murphy P; Francke U; Chen JD; Morgan G; Denton M; Greenberg CR; Wrogemann K; Blonden LA; van Paassen MB; van Ommen GJ; Kunkel LM
    Am J Hum Genet; 1989 Oct; 45(4):498-506. PubMed ID: 2491009
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Molecular and phenotypic analysis of patients with deletions within the deletion-rich region of the Duchenne muscular dystrophy (DMD) gene.
    Gillard EF; Chamberlain JS; Murphy EG; Duff CL; Smith B; Burghes AH; Thompson MW; Sutherland J; Oss I; Bodrug SE
    Am J Hum Genet; 1989 Oct; 45(4):507-20. PubMed ID: 2491010
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Localisation of the endpoints of deletions in the 5' region of the Duchenne gene using a sequence isolated by chromosome jumping.
    Kenwrick SJ; Smith TJ; England S; Collins F; Davies KE
    Nucleic Acids Res; 1988 Feb; 16(4):1305-17. PubMed ID: 3347492
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A small deletion in the Duchenne/Becker muscular dystrophy locus--a functionally important region?
    Hart KA; Monaco AP; Kunkel LM; Bobrow M
    Hum Genet; 1987 Sep; 77(1):88-91. PubMed ID: 3040577
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Gene deletions in X-linked muscular dystrophy.
    Lindlöf M; Kiuru A; Kääriäinen H; Kalimo H; Lang H; Pihko H; Rapola J; Somer H; Somer M; Savontaus ML
    Am J Hum Genet; 1989 Apr; 44(4):496-503. PubMed ID: 2929594
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Correlation of clinical and deletion data in Duchenne and Becker muscular dystrophy.
    Hodgson S; Hart K; Abbs S; Heckmatt J; Rodillo E; Bobrow M; Dubowitz V
    J Med Genet; 1989 Nov; 26(11):682-93. PubMed ID: 2585468
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A cDNA clone from the Duchenne/Becker muscular dystrophy gene.
    Burghes AH; Logan C; Hu X; Belfall B; Worton RG; Ray PN
    Nature; 1987 Jul 30-Aug 5; 328(6129):434-7. PubMed ID: 3614347
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. [Molecular genetic analysis of deletions in the Duchenne and Becker types of progressive muscular dystrophy].
    Kádasi L; Gécz J; Saksová L; Thurzová M
    Bratisl Lek Listy; 1993 May; 94(5):249-53. PubMed ID: 8173987
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Complete cloning of the Duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals.
    Koenig M; Hoffman EP; Bertelson CJ; Monaco AP; Feener C; Kunkel LM
    Cell; 1987 Jul; 50(3):509-17. PubMed ID: 3607877
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Analysis of molecular deletions with cDNA probes in patients with Duchenne and Becker muscular dystrophies.
    Gilgenkrantz H; Chelly J; Lambert M; Récan D; Barbot JC; van Ommen GJ; Kaplan JC
    Genomics; 1989 Oct; 5(3):574-80. PubMed ID: 2613240
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.