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 *

141 related articles for article (PubMed ID: 2253356)

  • 1. Determination of carrier status in Duchenne and Becker muscular dystrophies by quantitative polymerase chain reaction and allele-specific oligonucleotides.
    Prior TW; Papp AC; Snyder PJ; Highsmith WE; Friedman KJ; Perry TR; Silverman LM; Mendell JR
    Clin Chem; 1990 Dec; 36(12):2113-7. PubMed ID: 2253356
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Molecular probe protocol for determining carrier status in Duchenne and Becker muscular dystrophies.
    Prior TW; Friedman KJ; Highsmith WE; Perry TR; Silverman LM
    Clin Chem; 1990 Mar; 36(3):441-5. PubMed ID: 1968788
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A model for molecular screening of newborns: simultaneous detection of Duchenne/Becker muscular dystrophies and cystic fibrosis.
    Prior TW; Highsmith WE; Friedman KJ; Perry TR; Scheuerbrandt G; Silverman LM
    Clin Chem; 1990 Oct; 36(10):1756-9. PubMed ID: 2208650
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Carrier detection of Duchenne/Becker muscular dystrophy: computer-assisted direct quantitation of gene amplification products.
    Ishii K; Sakuraba H; Minamikawa-Tachino R; Shimmoto M; Suzuki Y
    Brain Dev; 1992 Mar; 14(2):80-3. PubMed ID: 1621929
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Detection of Duchenne and Becker muscular dystrophy carriers by quantitative multiplex polymerase chain reaction analysis.
    Ioannou P; Christopoulos G; Panayides K; Kleanthous M; Middleton L
    Neurology; 1992 Sep; 42(9):1783-90. PubMed ID: 1513470
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Carrier detection and microsatellite analysis of Duchenne and Becker muscular dystrophy in Spanish families.
    Kruyer H; Miranda M; Volpini V; Estivill X
    Prenat Diagn; 1994 Feb; 14(2):123-30. PubMed ID: 7910399
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Detection of 98% of DMD/BMD gene deletions by polymerase chain reaction.
    Beggs AH; Koenig M; Boyce FM; Kunkel LM
    Hum Genet; 1990 Nov; 86(1):45-8. PubMed ID: 2253937
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Detection of gene deletion in patients of Duchenne muscular dystrophy/Becker muscular dystrophy using polymerase chain reaction.
    Sinha S; Pradhan S; Mittal RD; Mittal B
    Indian J Med Res; 1992 Oct; 96():297-301. PubMed ID: 1459673
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Diagnosis of Duchenne/Becker muscular dystrophy and quantitative identification of carrier status by use of entangled solution capillary electrophoresis.
    Fortina P; Cheng J; Shoffner MA; Surrey S; Hitchcock WM; Kricka LJ; Wilding P
    Clin Chem; 1997 May; 43(5):745-51. PubMed ID: 9166226
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Detection of carriers of deletions in the dystrophin gene in Bulgarian DMD-BMD families.
    Bronzova J; Todorova A; Kalaydjieva L
    Hum Genet; 1994 Feb; 93(2):170-4. PubMed ID: 8112741
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Direct carrier detection by in situ suppression hybridization with cosmid clones of the Duchenne/Becker muscular dystrophy locus.
    Ried T; Mahler V; Vogt P; Blonden L; van Ommen GJ; Cremer T; Cremer M
    Hum Genet; 1990 Oct; 85(6):581-6. PubMed ID: 2227948
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Relatively low proportion of dystrophin gene deletions in Israeli Duchenne and Becker muscular dystrophy patients.
    Shomrat R; Gluck E; Legum C; Shiloh Y
    Am J Med Genet; 1994 Feb; 49(4):369-73. PubMed ID: 8160727
    [TBL] [Abstract][Full Text] [Related]  

  • 13. High frequency of de novo deletions in Mexican Duchenne and Becker muscular dystrophy patients. Implications for genetic counseling.
    Alcántara MA; Villarreal MT; Del Castillo V; Gutiérrez G; Saldaña Y; Maulen I; Lee R; Macías M; Orozco L
    Clin Genet; 1999 May; 55(5):376-80. PubMed ID: 10422811
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Fluorescent multiplex linkage analysis and carrier detection for Duchenne/Becker muscular dystrophy.
    Schwartz LS; Tarleton J; Popovich B; Seltzer WK; Hoffman EP
    Am J Hum Genet; 1992 Oct; 51(4):721-9. PubMed ID: 1415217
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Diagnosis of Duchenne and Becker muscular dystrophies by polymerase chain reaction. A multicenter study.
    Chamberlain JS; Chamberlain JR; Fenwick RG; Ward PA; Caskey CT; Dimnik LS; Bech-Hansen NT; Hoar DI; Richards S; Covone AE; Govanni R; Abbs S; Bentley DR; Bobrow M; Rysiecki G; Ray PN; Boileau C; Junien C; Boehm C; Venne VL; Fujmura FK; Spiga I; Ferrari M; Tedeschi S; Bakker E; Kneppers AL; van Ommen GJ; Jain K; Spector E; Crandall B; Kiuru A; Savontaus ML; Caskey CT; Chamberlain JS; Chamberlain JR; Rysiecki G
    JAMA; 1992 May; 267(19):2609-15. PubMed ID: 1573747
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Detection of deletions by the amplification of exons (multiplex PCR) in Duchenne muscular dystrophy].
    Claustres M; Kjellberg P; Desgeorges M; Bellet H; Sarda P; Bonnet H; Boileau C
    J Genet Hum; 1989 Sep; 37(3):251-7. PubMed ID: 2625628
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Deletion screening and carrier detection in Duchenne muscular dystrophy in Polish population via direct analysis of DNA and RNA transcripts.
    Kwiatkowska J; Lisiecka D; Sowinska J; Marszal E; Emich-Widera E; Ciesielski T; Szczególa-Przymusiak A; Nuc P; Chlebowska H; Zimowski J; Galas-Zgorzalewicz B; Slomski R
    Biochimie; 1997 Jul; 79(7):439-48. PubMed ID: 9352094
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Molecular diagnosis of Duchenne/Becker muscular dystrophy in Venezuelan patients with the polymerase chain reaction].
    Delgado Luengo W; Pineda-Del Villar L; Borjas L; Pons H; Morales A; Martínez Basalo MC; Saldaña HB
    Invest Clin; 1994 Dec; 35(4):195-207. PubMed ID: 7734522
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Deletion analysis of DMD/BMD children in Singapore using multiplex polymerase chain reaction (PCR) technique.
    Lai PS; Tay JS; Low PS; Lee WL; Koh GA; Gan GC
    J Trop Pediatr; 1992 Oct; 38(5):224-7. PubMed ID: 1433447
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Rapid detection of deletions in the Duchenne muscular dystrophy gene by PCR amplification of deletion-prone exon sequences.
    Hentemann M; Reiss J; Wagner M; Cooper DN
    Hum Genet; 1990 Feb; 84(3):228-32. PubMed ID: 2303244
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.