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 *

167 related articles for article (PubMed ID: 2893082)

  • 1. Prenatal testing for Duchenne and Becker muscular dystrophy.
    Cole CG; Walker A; Coyne A; Johnson L; Hart KA; Hodgson S; Sheridan R; Bobrow M
    Lancet; 1988 Feb; 1(8580):262-6. PubMed ID: 2893082
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. The diagnosis of Duchenne and Becker muscular dystrophies: two years' experience in a comprehensive carrier screening and prenatal diagnostic laboratory.
    Laing NG; Mears ME; Chandler DC; Layton MG; Thomas HE; Johnsen RD; Goldblatt J; Kakulas BA
    Med J Aust; 1991 Jan; 154(1):14-8. PubMed ID: 1670611
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The application of linkage analysis to genetic counselling in families with Duchenne or Becker muscular dystrophy.
    Hodgson S; Walker A; Cole C; Hart K; Johnson L; Heckmatt J; Dubowitz V; Bobrow M
    J Med Genet; 1987 Mar; 24(3):152-9. PubMed ID: 3572997
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Direct method for prenatal diagnosis and carrier detection in Duchenne/Becker muscular dystrophy using the entire dystrophin cDNA.
    Darras BT; Koenig M; Kunkel LM; Francke U
    Am J Med Genet; 1988 Mar; 29(3):713-26. PubMed ID: 2897793
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Prenatal diagnosis of Duchenne muscular dystrophy: a three-year experience in a rapidly evolving field.
    Bakker E; Bonten EJ; Veenema H; den Dunnen JT; Grootscholten PM; van Ommen GJ; Pearson PL
    J Inherit Metab Dis; 1989; 12 Suppl 1():174-90. PubMed ID: 2509804
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 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. Prenatal diagnosis of Duchenne muscular dystrophy by polymerase chain reaction analysis.
    Katayama S; Takeshita N; Yano T; Katagiri Y; Shirosita Y; Kubo H; Hirakawa S; Ubagai T
    Fetal Diagn Ther; 1994; 9(6):379-84. PubMed ID: 7880434
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Prenatal diagnosis in Becker muscular dystrophy.
    Wood S; Shukin RJ; Yong SL; Wilson D; Kalousek D; Chudley A
    Clin Genet; 1987 Jan; 31(1):45-7. PubMed ID: 2882880
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. 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]  

  • 14. [Prenatal diagnosis of Duchenne muscular dystrophy using DNA RFLP analysis].
    Zeng YT
    Zhonghua Yi Xue Za Zhi; 1988 Oct; 68(10):565-7, 38. PubMed ID: 2907413
    [No Abstract]   [Full Text] [Related]  

  • 15. Molecular biological approaches to genetic disorders in prenatal diagnosis.
    Katayama S
    Early Hum Dev; 1992; 29(1-3):149-53. PubMed ID: 1356752
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Prenatal diagnosis and carrier detection by DNA studies in a Duchenne muscular dystrophy family with no living affected male.
    Chen JD; Denton MJ; Serravalle S; Morgan G
    Aust Paediatr J; 1988 Dec; 24(6):351-3. PubMed ID: 2907402
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Prenatal diagnosis of Duchenne and Becker muscular dystrophy.
    Abbs S
    Prenat Diagn; 1996 Dec; 16(13):1187-98. PubMed ID: 9061750
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. [Carrier and prenatal diagnosis of Duchenne and Becker muscular dystrophy by PCR methods].
    Tsukamoto H; Inui K; Okada S
    Nihon Rinsho; 1993 Sep; 51(9):2428-34. PubMed ID: 8105117
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Prenatal DNA-diagnosis of Duchenne muscular dystrophy].
    Evgrafov OV; Poliakov AV; Zaĭtseva SP; Vinogradov SV; Bakharev VA; Mil'man FA; Lisova LP; Zaretskaia NV; Malygina NA; Badalian LO
    Mol Gen Mikrobiol Virusol; 1991 Feb; (2):15-6. PubMed ID: 1674355
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.