These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

73 related articles for article (PubMed ID: 2567785)

  • 21. [DNA-diagnosis of carriers of the Duchenne muscular dystrophy gene].
    Evgrafov OV; Poliakov AV; Zaĭtseva SP; Malygina NA; Badalian LO; Makarov VB
    Mol Gen Mikrobiol Virusol; 1990 Dec; (12):15-7. PubMed ID: 2084541
    [TBL] [Abstract][Full Text] [Related]  

  • 22. MspI RFLP for Duchenne muscular dystrophy cDNA subclone 9.
    Wagner M; Reiss J; Hentemann M; Thies U
    Nucleic Acids Res; 1989 Apr; 17(8):3328. PubMed ID: 2471152
    [No Abstract]   [Full Text] [Related]  

  • 23. Isolation of the gene for Duchenne muscular dystrophy.
    Singh DN
    Indian J Pediatr; 1988; 55(2):177-82. PubMed ID: 2900215
    [No Abstract]   [Full Text] [Related]  

  • 24. The use of linked DNA polymorphisms for genotype prediction in families with Duchenne muscular dystrophy.
    Harper PS; O'Brien T; Murray JM; Davies KE; Pearson P; Williamson R
    J Med Genet; 1983 Aug; 20(4):252-4. PubMed ID: 6684693
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Population variation in molecular polymorphisms of the short arm of the human X chromosome.
    Papiha SS; Mastana SS; Roberts DF; Onyemelukwe GC; Bhattacharya SS
    Am J Phys Anthropol; 1991 Jul; 85(3):329-34. PubMed ID: 1680294
    [TBL] [Abstract][Full Text] [Related]  

  • 26. 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]  

  • 27. Germline mosaicism and Duchenne muscular dystrophy mutations.
    Bakker E; Van Broeckhoven C; Bonten EJ; van de Vooren MJ; Veenema H; Van Hul W; Van Ommen GJ; Vandenberghe A; Pearson PL
    Nature; 1987 Oct 8-14; 329(6139):554-6. PubMed ID: 2889144
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [Uses of RFLP analysis in detecting Duchenne muscular dystrophy gene carrier].
    Chen F
    Zhonghua Yi Xue Za Zhi; 1991 Jun; 71(6):339-41. PubMed ID: 1687519
    [No Abstract]   [Full Text] [Related]  

  • 29. 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]  

  • 30. Duchenne muscular dystrophy (DMD) gene cDNA 8 PstI and TaqI polymorphisms involve exon 51 of the HindIII map.
    Laing NG; Akkari PA; Chandler DC; Thomas HE; Layton MG; Mears ME; Kakulas BA
    Nucleic Acids Res; 1990 Jul; 18(14):4284. PubMed ID: 1974044
    [No Abstract]   [Full Text] [Related]  

  • 31. [Application of RFLP analysis to Duchenne and Becker muscular dystrophy in Shandong Province. I. Carrier detections in females at risk].
    Guo Y; Wei J; Chen B; Cai F; Yang Y; Gong Y
    Yi Chuan Xue Bao; 1993; 20(1):12-8. PubMed ID: 8099495
    [TBL] [Abstract][Full Text] [Related]  

  • 32. RFLP for Duchenne muscular dystrophy cDNA clone 30-2.
    Walker AP; Bartlett RJ; Laing NG; Siddique T; Yamaoka LH; Chen JC; Hung WY; Roses AD
    Nucleic Acids Res; 1988 Sep; 16(18):9072. PubMed ID: 2902573
    [No Abstract]   [Full Text] [Related]  

  • 33. Molecular diagnosis of Duchenne muscular dystrophy by use of a conformational polymorphism in the absence of DNA from an affected boy.
    Tuffery S; Moine P; Sarda P; Lefort G; Boulot P; Demaille J; Claustres M
    Genet Couns; 1994; 5(2):183-5. PubMed ID: 7917130
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Service experience using DNA analysis for genetic prediction in Duchenne muscular dystrophy.
    Goodship J; Malcolm S; Robertson ME; Pembrey ME
    J Med Genet; 1988 Jan; 25(1):14-9. PubMed ID: 2895187
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Direct detection of more than 50% of the Duchenne muscular dystrophy mutations by field inversion gels.
    den Dunnen JT; Bakker E; Breteler EG; Pearson PL; van Ommen GJ
    Nature; 1987 Oct 15-21; 329(6140):640-2. PubMed ID: 2889148
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [Microsatellite analysis of Duchenne muscular dystrophy].
    Fujishita S; Shibuya N
    Nihon Rinsho; 1997 Dec; 55(12):3131-6. PubMed ID: 9436423
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Genetic linkage between Becker muscular dystrophy and a polymorphic DNA sequence on the short arm of the X chromosome.
    Kingston HM; Thomas NS; Pearson PL; Sarfarazi M; Harper PS
    J Med Genet; 1983 Aug; 20(4):255-8. PubMed ID: 6620324
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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]  

  • 39. Case of the month: germline mosaicism in carriers of Duchenne muscular dystrophy.
    Prior TW; Papp AC; Snyder PJ; Mendell JR
    Muscle Nerve; 1992 Aug; 15(8):960-3. PubMed ID: 1353862
    [TBL] [Abstract][Full Text] [Related]  

  • 40. The screening of Duchenne muscular dystrophy patients for submicroscopic deletions.
    Hart K; Cole C; Walker A; Hodgson S; Johnson L; Dubowitz V; Ray P; Worton R; Bobrow M
    J Med Genet; 1986 Dec; 23(6):516-20. PubMed ID: 3806637
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 4.