BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

180 related articles for article (PubMed ID: 2570527)

  • 1. Hot spot of recombination within DXS164 in the Duchenne muscular dystrophy gene.
    Grimm T; Müller B; Dreier M; Kind E; Bettecken T; Meng G; Müller CR
    Am J Hum Genet; 1989 Sep; 45(3):368-72. PubMed ID: 2570527
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A genetic linkage map of five marker loci in and around the Duchenne muscular dystrophy locus.
    Chen JD; Hejtmancik JF; Romeo G; Lindlof M; Boehm C; Caskey CT; Kress W; Fischbeck KH; Dreier M; Serravalle S
    Genomics; 1989 Jan; 4(1):105-9. PubMed ID: 2563349
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Localization and cloning of Xp21 deletion breakpoints involved in muscular dystrophy.
    Monaco AP; Bertelson CJ; Colletti-Feener C; Kunkel LM
    Hum Genet; 1987 Mar; 75(3):221-7. PubMed ID: 2881877
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Linked polymorphic DNA markers in the prediction of X-linked muscular dystrophy.
    Lindlöf M; Sistonen P; de la Chapelle A
    Ann Hum Genet; 1987 Oct; 51(4):317-28. PubMed ID: 3482147
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Genetic linkage relationships of seven DNA probes with Duchenne and Becker muscular dystrophy.
    Brown CS; Thomas NS; Sarfarazi M; Davies KE; Kunkel L; Pearson PL; Kingston HM; Shaw DJ; Harper PS
    Hum Genet; 1985; 71(1):62-74. PubMed ID: 2993158
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Localisation of Xp21 meiotic exchange points in Duchenne muscular dystrophy families.
    Bertelson CJ; Bartley JA; Monaco AP; Colletti-Feener C; Fischbeck K; Kunkel LM
    J Med Genet; 1986 Dec; 23(6):531-7. PubMed ID: 2879924
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Segregation analysis of a marker localised Xp21.2-Xp21.3 in Duchenne and Becker muscular dystrophy families.
    Dorkins H; Junien C; Mandel JL; Wrogemann K; Moison JP; Martinez M; Old JM; Bundey S; Schwartz M; Carpenter N
    Hum Genet; 1985; 71(2):103-7. PubMed ID: 2995231
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Accurate assessment of intragenic recombination frequency within the Duchenne muscular dystrophy gene.
    Abbs S; Roberts RG; Mathew CG; Bentley DR; Bobrow M
    Genomics; 1990 Aug; 7(4):602-6. PubMed ID: 1974880
    [TBL] [Abstract][Full Text] [Related]  

  • 9. DNA probe analysis for carrier detection and prenatal diagnosis of Duchenne muscular dystrophy: a standard diagnostic procedure.
    Bakker E; Bonten EJ; De Lange LF; Veenema H; Majoor-Krakauer D; Hofker MH; Van Ommen GJ; Pearson PL
    J Med Genet; 1986 Dec; 23(6):573-80. PubMed ID: 2879929
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Human X chromosome markers and Duchenne muscular dystrophy.
    Davies KE; Speer A; Herrmann F; Spiegler AW; McGlade S; Hofker MH; Briand P; Hanke R; Schwartz M; Steinbicker V
    Nucleic Acids Res; 1985 May; 13(10):3419-26. PubMed ID: 3859837
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Multipoint linkage analysis of the short arm of the human X chromosome in families with X-linked muscular dystrophy.
    Wilcox DE; Affara NA; Yates JR; Ferguson-Smith MA; Pearson PL
    Hum Genet; 1985; 70(4):365-75. PubMed ID: 3860471
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Linkage studies in Duchenne and Becker muscular dystrophies.
    Walker A; Hart K; Cole C; Hodgson S; Johnson L; Dubowitz V; Bobrow M
    J Med Genet; 1986 Dec; 23(6):538-47. PubMed ID: 2879925
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Isolation of candidate cDNAs for portions of the Duchenne muscular dystrophy gene.
    Monaco AP; Neve RL; Colletti-Feener C; Bertelson CJ; Kurnit DM; Kunkel LM
    Nature; 1986 Oct 16-22; 323(6089):646-50. PubMed ID: 3773991
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Linkage analysis of polymorphisms within the DNA fragment XJ cloned from the breakpoint of an X;21 translocation associated with X linked muscular dystrophy.
    Thompson MW; Ray PN; Belfall B; Duff C; Logan C; Oss I; Worton RG
    J Med Genet; 1986 Dec; 23(6):548-55. PubMed ID: 2879926
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Genetic linkage study between the loci for Duchenne and Becker muscular dystrophy and nine X-chromosomal DNA markers.
    Wilichowski E; Krawczak M; Seemanova E; Hanefeld F; Schmidtke J
    Hum Genet; 1987 Jan; 75(1):32-40. PubMed ID: 3026946
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Familial inheritance of a DXS164 deletion mutation from a heterozygous female.
    Lanman JT; Pericak-Vance MA; Bartlett RJ; Chen JC; Yamaoka L; Koh J; Speer MC; Hung WY; Roses AD
    Am J Hum Genet; 1987 Aug; 41(2):138-44. PubMed ID: 2887110
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Isolation of probes detecting restriction fragment length polymorphisms from X chromosome-specific libraries: potential use for diagnosis of Duchenne muscular dystrophy.
    Hofker MH; Wapenaar MC; Goor N; Bakker E; van Ommen GJ; Pearson PL
    Hum Genet; 1985; 70(2):148-56. PubMed ID: 2989153
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genetic linkage relationship between the Xg blood group system and two X chromosome DNA polymorphisms in families with Duchenne and Becker muscular dystrophy.
    Sarfarazi M; Harper PS; Kingston HM; Murray JM; O'Brien T; Davies KE; Williamson R; Tippett P; Sanger R
    Hum Genet; 1983; 65(2):169-71. PubMed ID: 6317539
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Isolation of a random cosmid clone, cX5, which defines a new polymorphic locus DXS148 near the locus for Duchenne muscular dystrophy.
    Hofker MH; Bergen AA; Skraastad MI; Bakker E; Francke U; Wieringa B; Bartley J; van Ommen GJ; Pearson PL
    Hum Genet; 1986 Nov; 74(3):275-9. PubMed ID: 2877936
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 9.