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4. Analysis of RFLPs and DNA deletions in the Chinese Duchenne muscular dystrophy gene. Zeng YT; Chen MJ; Ren ZR; Qui XK; Huang SZ J Med Genet; 1991 Mar; 28(3):167-70. PubMed ID: 1675685 [TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. RFLPs for Duchenne muscular dystrophy cDNA clones 9 and 10. Liechti-Gallati S; Schneider V; Mullis P; Moser H Am J Hum Genet; 1990 Jun; 46(6):1090-4. PubMed ID: 1971151 [TBL] [Abstract][Full Text] [Related]
8. Significantly higher frequency of the MspI 2.2 kb allele of the Duchenne muscular dystrophy intragenic probe P-20 in the Chinese population. Wei J; Guo Y; Chen B; Yang Y Hum Genet; 1992; 90(1-2):149-50. PubMed ID: 1385293 [TBL] [Abstract][Full Text] [Related]
9. Molecular deletion analysis in Duchenne muscular dystrophy. Thomas NS; Ray PN; Worton RG; Harper PS J Med Genet; 1986 Dec; 23(6):509-15. PubMed ID: 2879923 [TBL] [Abstract][Full Text] [Related]
10. TaqL and MspL RFLPs are detected by the human 2,3-biphosphoglycerate mutase (BPGM) cDNA. Dracopoli NC; Feltquate DM; Sam B; Schartl M Nucleic Acids Res; 1990 Apr; 18(7):1928. PubMed ID: 1692409 [No Abstract] [Full Text] [Related]
11. A rare MspI RFLP of the DMD probe p20 (DXS269). Uhlhaas S; Bakker E; van Broeckhoven C; Barth-Schulz A; Friedl W Hum Genet; 1992 Apr; 89(1):122. PubMed ID: 1374360 [No Abstract] [Full Text] [Related]
12. Topography of the Duchenne muscular dystrophy (DMD) gene: FIGE and cDNA analysis of 194 cases reveals 115 deletions and 13 duplications. Den Dunnen JT; Grootscholten PM; Bakker E; Blonden LA; Ginjaar HB; Wapenaar MC; van Paassen HM; van Broeckhoven C; Pearson PL; van Ommen GJ Am J Hum Genet; 1989 Dec; 45(6):835-47. PubMed ID: 2573997 [TBL] [Abstract][Full Text] [Related]
13. DNA probes for carrier identification in Duchenne muscular dystrophy. Worton RG Clin Chem; 1989 Apr; 35(4):519-20. PubMed ID: 2564816 [No Abstract] [Full Text] [Related]
14. Normal human genomic restriction-fragment patterns and polymorphisms revealed by hybridization with the entire dystrophin cDNA. Darras BT; Francke U Am J Hum Genet; 1988 Nov; 43(5):612-9. PubMed ID: 2903662 [TBL] [Abstract][Full Text] [Related]
15. Molecular deletion patterns in Duchenne and Becker type muscular dystrophy. Liechti-Gallati S; Koenig M; Kunkel LM; Frey D; Boltshauser E; Schneider V; Braga S; Moser H Hum Genet; 1989 Mar; 81(4):343-8. PubMed ID: 2784778 [TBL] [Abstract][Full Text] [Related]
16. Use of DNA probes in detecting carriers of Duchenne muscular dystrophy: selected case studies. Prior TW; Blasco PA; Dove JL; Leshner RT; Gruemer HD Clin Chem; 1989 Apr; 35(4):679-83. PubMed ID: 2564818 [TBL] [Abstract][Full Text] [Related]
17. 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]