128 related articles for article (PubMed ID: 3562224)
1. Isolation of a conserved sequence deleted in Duchenne muscular dystrophy patients.
Smith TJ; Wilson L; Kenwrick SJ; Forrest SM; Speer A; Coutelle C; Davies KE
Nucleic Acids Res; 1987 Mar; 15(5):2167-74. PubMed ID: 3562224
[TBL] [Abstract][Full Text] [Related]
2. Mapping of 12 translocation breakpoints in the Xp21 region with respect to the locus for Duchenne muscular dystrophy.
Boyd Y; Cockburn D; Holt S; Munro E; Van Ommen GJ; Gillard B; Affara N; Ferguson-Smith M; Craig I
Cytogenet Cell Genet; 1988; 48(1):28-34. PubMed ID: 3180845
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Conservation of the Duchenne muscular dystrophy gene in mice and humans.
Hoffman EP; Monaco AP; Feener CC; Kunkel LM
Science; 1987 Oct; 238(4825):347-50. PubMed ID: 3659917
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Mapping of four translocation breakpoints within the Duchenne muscular dystrophy gene.
Bodrug SE; Burghes AH; Ray PM; Worton RG
Genomics; 1989 Jan; 4(1):101-4. PubMed ID: 2914705
[TBL] [Abstract][Full Text] [Related]
7. Duchenne muscular dystrophy (DMD) in a female with an X/autosome translocation: further evidence that the DMD locus is at Xp21.
Jacobs PA; Hunt PA; Mayer M; Bart RD
Am J Hum Genet; 1981 Jul; 33(4):513-8. PubMed ID: 7258185
[TBL] [Abstract][Full Text] [Related]
8. Duchenne and Becker muscular dystrophy mutations: analysis using 2.6 kb of muscle cDNA from the 5' end of the gene.
Smith TJ; Forrest SM; Cross GS; Davies KE
Nucleic Acids Res; 1987 Dec; 15(23):9761-9. PubMed ID: 3697082
[TBL] [Abstract][Full Text] [Related]
9. Isolation of candidate cDNAs for portions of the Duchenne muscular dystrophy gene.
Monaco AP; Neve RL; Colletti-Feener C; Bertelson CJ; Kurnit DM; Kunkel LM
Nature; 1986 Oct 16-22; 323(6089):646-50. PubMed ID: 3773991
[TBL] [Abstract][Full Text] [Related]
10. Mild and severe muscular dystrophy associated with deletions in Xp21 of the human X chromosome.
Davies KE; Smith TJ; Bundey S; Read AP; Flint T; Bell M; Speer A
J Med Genet; 1988 Jan; 25(1):9-13. PubMed ID: 3162536
[TBL] [Abstract][Full Text] [Related]
11. Common sequence motifs at the rearrangement sites of a constitutional X/autosome translocation and associated deletion.
Giacalone JP; Francke U
Am J Hum Genet; 1992 Apr; 50(4):725-41. PubMed ID: 1347968
[TBL] [Abstract][Full Text] [Related]
12. Muscular dystrophy in girls with X;autosome translocations.
Boyd Y; Buckle V; Holt S; Munro E; Hunter D; Craig I
J Med Genet; 1986 Dec; 23(6):484-90. PubMed ID: 3806636
[TBL] [Abstract][Full Text] [Related]
13. The screening of Duchenne muscular dystrophy patients for submicroscopic deletions.
Hart K; Cole C; Walker A; Hodgson S; Johnson L; Dubowitz V; Ray P; Worton R; Bobrow M
J Med Genet; 1986 Dec; 23(6):516-20. PubMed ID: 3806637
[TBL] [Abstract][Full Text] [Related]
14. Molecular analysis of a constitutional X-autosome translocation in a female with muscular dystrophy.
Bodrug SE; Ray PN; Gonzalez IL; Schmickel RD; Sylvester JE; Worton RG
Science; 1987 Sep; 237(4822):1620-4. PubMed ID: 3629260
[TBL] [Abstract][Full Text] [Related]
15. Translocation (X;6) in a female with Duchenne muscular dystrophy: implications for the localisation of the DMD locus.
Zatz M; Vianna-Morgante AM; Campos P; Diament AJ
J Med Genet; 1981 Dec; 18(6):442-7. PubMed ID: 7334502
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Further evidence for Xp21 location of Duchenne muscular dystrophy (DMD) locus: X;9 translocation in a female with DMD.
Emanuel BS; Zackai EH; Tucker SH
J Med Genet; 1983 Dec; 20(6):461-3. PubMed ID: 6655672
[TBL] [Abstract][Full Text] [Related]
18. Duchenne muscular dystrophy. Collaboration and progress.
Goodfellow PN
Nature; 1986 Jul 3-9; 322(6074):12-3. PubMed ID: 3724849
[No Abstract] [Full Text] [Related]
19. Xp21/autosome translocations. Case report and risk for Duchenne muscular dystrophy.
Holden JJ; Smith A; MacLeod PM; Masotti R; Duncan AM
Clin Genet; 1986 Jun; 29(6):516-22. PubMed ID: 3742857
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]