BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

462 related articles for article (PubMed ID: 2989153)

  • 1. 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]  

  • 2. 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]  

  • 3. Prenatal diagnosis and carrier detection of Duchenne muscular dystrophy with closely linked RFLPs.
    Bakker E; Hofker MH; Goor N; Mandel JL; Wrogemann K; Davies KE; Kunkel LM; Willard HF; Fenton WA; Sandkuyl L
    Lancet; 1985 Mar; 1(8430):655-8. PubMed ID: 2858615
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Carrier diagnosis of Duchenne muscular dystrophy using restriction fragment length polymorphisms.
    Hejtmancik JF; Harris SG; Tsao CC; Ward PA; Caskey CT
    Neurology; 1986 Dec; 36(12):1553-62. PubMed ID: 2878392
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Carrier detection and prenatal diagnosis in X linked muscular dystrophy using restriction fragment length polymorphisms.
    Lindlöf M; Kääriäinen H; Davies KE; de la Chapelle A
    J Med Genet; 1986 Dec; 23(6):560-72. PubMed ID: 2879928
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Development of additional RFLP probes near the locus for Duchenne muscular dystrophy by cosmid cloning of the DXS84 (754) locus.
    Hofker MH; van Ommen GJ; Bakker E; Burmeister M; Pearson PL
    Hum Genet; 1986 Nov; 74(3):270-4. PubMed ID: 2877935
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Linkage analysis of a DNA polymorphism proximal to the Duchenne and Becker muscular dystrophy loci on the short arm of the X chromosome.
    Brown CS; Pearson PL; Thomas NS; Sarfarazi M; Harper PS; Shaw DJ
    J Med Genet; 1985 Jun; 22(3):179-81. PubMed ID: 2989525
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. 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]  

  • 12. Prenatal diagnosis and carrier detection of Duchenne muscular dystrophy by restriction fragment length polymorphism analysis with pERT 87 deoxyribonucleic acid probes.
    Katayama S; Montano M; Slotnick RN; Lebo RV; Golbus MS
    Am J Obstet Gynecol; 1988 Mar; 158(3 Pt 1):548-55. PubMed ID: 2894769
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A new probe for the diagnosis of myotonic muscular dystrophy.
    Bartlett RJ; Pericak-Vance MA; Yamaoka L; Gilbert J; Herbstreith M; Hung WY; Lee JE; Mohandas T; Bruns G; Laberge C
    Science; 1987 Mar; 235(4796):1648-50. PubMed ID: 3029876
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 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. Localization of DNA sequences in region Xp21 of the human X chromosome: search for molecular markers close to the Duchenne muscular dystrophy locus.
    de Martinville B; Kunkel LM; Bruns G; Morlé F; Koenig M; Mandel JL; Horwich A; Latt SA; Gusella JF; Housman D
    Am J Hum Genet; 1985 Mar; 37(2):235-49. PubMed ID: 2984924
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Molecular-genetic study of Duchenne and Becker muscular dystrophies: deletion analyses of 45 Japanese patients and segregation analyses in their families with RFLPs based on the data from normal Japanese females.
    Sugino S; Fujishita S; Kamimura N; Matsumoto T; Wapenaar MC; Deng HX; Shibuya N; Miike T; Niikawa N
    Am J Med Genet; 1989 Dec; 34(4):555-61. PubMed ID: 2576185
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Prenatal diagnosis of Duchenne muscular dystrophy by DNA analysis.
    Old JM; Davies KE
    J Med Genet; 1986 Dec; 23(6):556-9. PubMed ID: 2879927
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Definitive localization of Becker muscular dystrophy in Xp by linkage to a cluster of DNA polymorphisms (DXS43 and DXS9).
    Fadda S; Mochi M; Roncuzzi L; Sangiorgi S; Sbarra D; Zatz M; Romeo G
    Hum Genet; 1985; 71(1):33-6. PubMed ID: 2993155
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 24.