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 *

125 related articles for article (PubMed ID: 3358426)

  • 1. The use of field-inversion gel electrophoresis for deletion detection in Duchenne muscular dystrophy.
    Chen JD; Denton MJ; Morgan G; Pearn JH; Mackinlay AG
    Am J Hum Genet; 1988 May; 42(5):777-80. PubMed ID: 3358426
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Possibilities and limitations of carrier diagnosis in families with Duchenne muscular dystrophy caused by deletions in the major hot spot region using pulsed-field gel electrophoresis.
    Huschenbett J; Volz A; Pfeifer L; Speer A
    Biomed Biochim Acta; 1991; 50(12):1205-12. PubMed ID: 1824538
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Identification of a 220-kb insertion into the Duchenne gene in a family with an atypical course of muscular dystrophy.
    Bettecken T; Müller CR
    Genomics; 1989 May; 4(4):592-6. PubMed ID: 2568331
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Analysis of deletions in DNA from patients with Becker and Duchenne muscular dystrophy.
    Kunkel LM; Hejtmancik JF; Caskey CT; Speer A; Monaco AP; Middlesworth W; Colletti CA; Bertelson C; Müller U; Bresnan M; Shapiro F; Tantravahi U; Speer J; Latt SA; Bartlett R; Pericak-Vance MA; Roses AD; Thompson MW; Ray PN; Worton RG; Fischbeck KH; Gallano P; Coulon M; Duros C; Boue J; Junien C; Chelly J; Hamard G; Jeanpierre M; Lambert M; Kaplan JC; Emery A; Dorkins H; McGlade S; Davies KE; Boehm C; Arveiler B; Lemaire C; Morgan GJ; Denton MJ; Amos J; Bobrow M; Benham F; Boswinkel E; Cole C; Dubowitz V; Hart K; Hodgson S; Johnson L; Walker A; Roncuzzi L; Ferlini A; Nobile C; Romeo G; Wilcox DE; Affara NA; Ferguson-Smith MA; Lindolf M; Kaariainen H; de la Chapelle A; Ionasescu V; Searby C; Ionasescu R; Bakker E; van Ommen GJ; Pearson PL; Greenberg CR; Hamerton JL; Wrogemann K; Doherty RA; Polakowska R; Hyser C; Quirk S; Thomas N; Harper JF; Darras BT; Francke U
    Nature; 1986 Jul 3-9; 322(6074):73-7. PubMed ID: 3014348
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Long-range genomic map of the Duchenne muscular dystrophy (DMD) gene: isolation and use of J66 (DXS268), a distal intragenic marker.
    van Ommen GJ; Bertelson C; Ginjaar HB; den Dunnen JT; Bakker E; Chelly J; Matton M; van Essen AJ; Bartley J; Kunkel LM
    Genomics; 1987 Dec; 1(4):329-36. PubMed ID: 2896627
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Detection of Duchenne muscular dystrophy carriers by dosage analysis using the DMD cDNA clone 8.
    Mao YP; Cremer M
    Hum Genet; 1989 Jan; 81(2):193-5. PubMed ID: 2912889
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Molecular analysis of the Duchenne muscular dystrophy region using pulsed field gel electrophoresis.
    Kenwrick S; Patterson M; Speer A; Fischbeck K; Davies K
    Cell; 1987 Jan; 48(2):351-7. PubMed ID: 3026644
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Further studies of gene deletions that cause Duchenne and Becker muscular dystrophies.
    Forrest SM; Cross GS; Flint T; Speer A; Robson KJ; Davies KE
    Genomics; 1988 Feb; 2(2):109-14. PubMed ID: 3410474
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Clones from an 840-kb fragment containing the 5' region of the DMD locus enriched by pulsed field gel electrophoresis.
    Anand R; Honeycombe J; Whittaker PA; Elder JK; Southern EM
    Genomics; 1988 Oct; 3(3):177-86. PubMed ID: 3066744
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Physical mapping distal to the DMD locus.
    Love DR; Bloomfield JF; Kenwrick SJ; Yates JR; Davies KE
    Genomics; 1990 Sep; 8(1):106-12. PubMed ID: 2081587
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genetic abnormalities in Duchenne and Becker dystrophies: clinical correlations.
    Medori R; Brooke MH; Waterston RH
    Neurology; 1989 Apr; 39(4):461-5. PubMed ID: 2648185
    [TBL] [Abstract][Full Text] [Related]  

  • 12. DNA studies in a family with Duchenne muscular dystrophy and a deletion at Xp21.
    Greenberg CR; Hamerton JL; Nigli M; Wrogemann K
    Am J Hum Genet; 1987 Aug; 41(2):128-37. PubMed ID: 3475976
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Localisation of the endpoints of deletions in the 5' region of the Duchenne gene using a sequence isolated by chromosome jumping.
    Kenwrick SJ; Smith TJ; England S; Collins F; Davies KE
    Nucleic Acids Res; 1988 Feb; 16(4):1305-17. PubMed ID: 3347492
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Use of dystrophin c-DNA for the direct diagnosis of Duchenne muscular dystrophy in female carriers].
    Baiget M; del Río E; Gallano P
    Neurologia; 1989 Oct; 4(8):268-76. PubMed ID: 2576910
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A deletion hot spot in the Duchenne muscular dystrophy gene.
    Wapenaar MC; Kievits T; Hart KA; Abbs S; Blonden LA; den Dunnen JT; Grootscholten PM; Bakker E; Verellen-Dumoulin C; Bobrow M
    Genomics; 1988 Feb; 2(2):101-8. PubMed ID: 2900805
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Duchenne muscular dystrophy: high frequency of deletions.
    Bartlett RJ; Pericak-Vance MA; Koh J; Yamaoka LH; Chen JC; Hung WY; Speer MC; Wapenaar MC; Van Ommen GJ; Bakker E
    Neurology; 1988 Jan; 38(1):1-4. PubMed ID: 3275902
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Molecular biology in diagnosis and detection of deletion in Duchenne muscular dystrophy].
    Graninger W; Wintersberger W; Meron G; Smolen J; Toifl K; Vormittag W
    Wien Klin Wochenschr; 1991; 103(7):207-9. PubMed ID: 2063586
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A cDNA clone from the Duchenne/Becker muscular dystrophy gene.
    Burghes AH; Logan C; Hu X; Belfall B; Worton RG; Ray PN
    Nature; 1987 Jul 30-Aug 5; 328(6129):434-7. PubMed ID: 3614347
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Intragenic deletions in 21 Duchenne muscular dystrophy (DMD)/Becker muscular dystrophy (BMD) families studied with the dystrophin cDNA: location of breakpoints on HindIII and BglII exon-containing fragment maps, meiotic and mitotic origin of the mutations.
    Darras BT; Blattner P; Harper JF; Spiro AJ; Alter S; Francke U
    Am J Hum Genet; 1988 Nov; 43(5):620-9. PubMed ID: 2903663
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.