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 *

137 related articles for article (PubMed ID: 3458666)

  • 21. 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]  

  • 22. Application of DNA probes to carrier detection and prenatal diagnosis of Duchenne (and Becker) muscular dystrophy.
    Mulley JC; Gedeon AK; Haan EA; Sheffield LJ; White SJ; Bates LJ; Robertson EF; Sutherland GR
    Aust Paediatr J; 1988; 24 Suppl 1():92-7. PubMed ID: 3202740
    [TBL] [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. 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]  

  • 25. Mapping DNA sequences in a human X-chromosome deletion which extends across the region of the Duchenne muscular dystrophy mutation.
    Ingle C; Williamson R; de la Chapelle A; Herva RR; Haapala K; Bates G; Willard HF; Pearson P; Davies KE
    Am J Hum Genet; 1985 May; 37(3):451-62. PubMed ID: 2988331
    [TBL] [Abstract][Full Text] [Related]  

  • 26. 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]  

  • 27. 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]  

  • 28. The genetic linkage map of the human X chromosome.
    Drayna D; White R
    Science; 1985 Nov; 230(4727):753-8. PubMed ID: 4059909
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Deletion analysis for Duchenne (and Becker) muscular dystrophy.
    Kimber RD; Hyland VJ; Haan EA; Mulley JC
    Aust Paediatr J; 1989 Oct; 25(5):292-5. PubMed ID: 2590130
    [TBL] [Abstract][Full Text] [Related]  

  • 30. 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]  

  • 31. Molecular analysis of human muscular dystrophies.
    Davies KE; Forrest S; Smith T; Kenwrick S; Ball S; Dorkins H; Patterson M
    Muscle Nerve; 1987; 10(3):191-9. PubMed ID: 2882417
    [TBL] [Abstract][Full Text] [Related]  

  • 32. A 10-megabase physical map of human Xp21, including the Duchenne muscular dystrophy gene.
    Burmeister M; Monaco AP; Gillard EF; van Ommen GJ; Affara NA; Ferguson-Smith MA; Kunkel LM; Lehrach H
    Genomics; 1988 Apr; 2(3):189-202. PubMed ID: 3397058
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Easy calculations of lod scores and genetic risks on small computers.
    Lathrop GM; Lalouel JM
    Am J Hum Genet; 1984 Mar; 36(2):460-5. PubMed ID: 6585139
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [Diagnosis of Duchenne muscular dystrophy using DNA probes].
    Evgrafov OV; Makarov VB
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1987; 87(11):1732-6. PubMed ID: 3324590
    [No Abstract]   [Full Text] [Related]  

  • 35. 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]  

  • 36. 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]  

  • 37. 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]  

  • 38. Microdeletions in patients with X-linked muscular dystrophy: molecular-clinical correlations.
    Lindlöf M; Kääriäinen H; van Ommen GJ; de la Chapelle A
    Clin Genet; 1988 Feb; 33(2):131-9. PubMed ID: 3162851
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Molecular analysis of muscular dystrophy.
    Davies KE; Kenwrick SJ; Patterson MN; Smith TJ; Forrest SM; Dorkins HR; Cross GS; England SB
    J Muscle Res Cell Motil; 1988 Feb; 9(1):1-8. PubMed ID: 3292577
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Regional localisation of X chromosome short arm probes.
    Paulsen K; Forrest S; Scherer G; Ropers HH; Davies K
    Hum Genet; 1986 Oct; 74(2):155-9. PubMed ID: 3464558
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.