186 related articles for article (PubMed ID: 10924480)
21. Analysis of 22 deletion breakpoints in dystrophin intron 49.
Nobile C; Toffolatti L; Rizzi F; Simionati B; Nigro V; Cardazzo B; Patarnello T; Valle G; Danieli GA
Hum Genet; 2002 May; 110(5):418-21. PubMed ID: 12073011
[TBL] [Abstract][Full Text] [Related]
22. [Carrier genetic diagnosis of intron and/or exon-deletion Duchenne muscular dystrophy by microsatellite analysis and quantitative polymerase chain reaction].
Huang W; Zhang C; Xie YM; Chen SL; Zhang WX; Yao XL; Zeng Y; Lu XL
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Feb; 24(1):72-5. PubMed ID: 17285549
[TBL] [Abstract][Full Text] [Related]
23. Splicing mutation of a gene within the Duchenne muscular dystrophy family.
Zhu YB; Gan JH; Luo JW; Zheng XY; Wei SC; Hu D
Genet Mol Res; 2016 Jul; 15(2):. PubMed ID: 27421007
[TBL] [Abstract][Full Text] [Related]
24. Nucleotide variation at the runt locus in Drosophila melanogaster and Drosophila simulans.
Labate JA; Biermann CH; Eanes WF
Mol Biol Evol; 1999 Jun; 16(6):724-31. PubMed ID: 10368951
[TBL] [Abstract][Full Text] [Related]
25. Cloning and sequencing of junction fragment with exons 45-54 deletion of dystrophin gene.
Zhong M; Pan SY; Lu BX; Li W
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2006 Apr; 23(2):138-41. PubMed ID: 16604481
[TBL] [Abstract][Full Text] [Related]
26. Linkage disequilibria among (CA)n polymorphisms in the human dystrophin gene and their implications in carrier detection and prenatal diagnosis in Duchenne and Becker muscular dystrophies.
Chakraborty R; Zhong Y; de Andrade M; Clemens PR; Fenwick RG; Caskey CT
Genomics; 1994 Jun; 21(3):567-70. PubMed ID: 7959733
[TBL] [Abstract][Full Text] [Related]
27. Tissue- and case-specific retention of intron 40 in mature dystrophin mRNA.
Nishida A; Minegishi M; Takeuchi A; Niba ET; Awano H; Lee T; Iijima K; Takeshima Y; Matsuo M
J Hum Genet; 2015 Jun; 60(6):327-33. PubMed ID: 25833469
[TBL] [Abstract][Full Text] [Related]
28. Polymorphisms of three new microsatellite sites of the dystrophin gene.
Sun RF; Zhu YS; Feng JL; Tian Z; Kuang WJ; Liu Y; Zhang HB; Li SB
Genet Mol Res; 2011 Apr; 10(2):744-51. PubMed ID: 21523654
[TBL] [Abstract][Full Text] [Related]
29. Estimates of linkage disequilibrium and the recombination parameter determined from segregating nucleotide sites in the alcohol dehydrogenase region of Drosophila pseudoobscura.
Schaeffer SW; Miller EL
Genetics; 1993 Oct; 135(2):541-52. PubMed ID: 8244013
[TBL] [Abstract][Full Text] [Related]
30. Precise mapping of 17 deletion breakpoints within the central hotspot deletion region (introns 50 and 51) of the DMD gene.
Esposito G; Tremolaterra MR; Marsocci E; Tandurella IC; Fioretti T; Savarese M; Carsana A
J Hum Genet; 2017 Dec; 62(12):1057-1063. PubMed ID: 28878337
[TBL] [Abstract][Full Text] [Related]
31. Genetic analysis of 62 Chinese families with Duchenne muscular dystrophy and strategies of prenatal diagnosis in a single center.
Zhang J; Ma D; Liu G; Wang Y; Liu A; Li L; Luo C; Hu P; Xu Z
BMC Med Genet; 2019 Nov; 20(1):180. PubMed ID: 31727011
[TBL] [Abstract][Full Text] [Related]
32. Prenatal diagnosis of Duchenne muscular dystrophy revealed a novel mosaic mutation in Dystrophin gene: a case report.
Wang Y; Chen Y; Wang SM; Liu X; Gu YN; Feng Z
BMC Med Genet; 2020 Nov; 21(1):222. PubMed ID: 33176713
[TBL] [Abstract][Full Text] [Related]
33. Duchenne and Becker muscular dystrophy: a molecular and immunohistochemical approach.
Freund AA; Scola RH; Arndt RC; Lorenzoni PJ; Kay CK; Werneck LC
Arq Neuropsiquiatr; 2007 Mar; 65(1):73-6. PubMed ID: 17420831
[TBL] [Abstract][Full Text] [Related]
34. Genetic diagnosis of Duchenne/Becker muscular dystrophy using next-generation sequencing: validation analysis of DMD mutations.
Okubo M; Minami N; Goto K; Goto Y; Noguchi S; Mitsuhashi S; Nishino I
J Hum Genet; 2016 Jun; 61(6):483-9. PubMed ID: 26911353
[TBL] [Abstract][Full Text] [Related]
35. Non-homologous recombination between Alu and LINE-1 repeats caused a 430-kb deletion in the dystrophin gene: a novel source of genomic instability.
Suminaga R; Takeshima Y; Yasuda K; Shiga N; Nakamura H; Matsuo M
J Hum Genet; 2000; 45(6):331-6. PubMed ID: 11185740
[TBL] [Abstract][Full Text] [Related]
36. Intronic Alternative Polyadenylation in the Middle of the
Rani AQM; Yamamoto T; Kawaguchi T; Maeta K; Awano H; Nishio H; Matsuo M
Int J Mol Sci; 2020 May; 21(10):. PubMed ID: 32443516
[TBL] [Abstract][Full Text] [Related]
37. A novel cryptic exon in intron 3 of the dystrophin gene was incorporated into dystrophin mRNA with a single nucleotide deletion in exon 5.
Suminaga R; Takeshima Y; Adachi K; Yagi M; Nakamura H; Matsuo M
J Hum Genet; 2002; 47(4):196-201. PubMed ID: 12166656
[TBL] [Abstract][Full Text] [Related]
38. The dystrophin / utrophin homologues in Drosophila and in sea urchin.
Neuman S; Kaban A; Volk T; Yaffe D; Nudel U
Gene; 2001 Jan; 263(1-2):17-29. PubMed ID: 11223239
[TBL] [Abstract][Full Text] [Related]
39. [Genetic analysis and prenatal diagnosis of Duchenne or Becker muscular dystrophy].
Zhao W; Jiang N; Li S; Li JS; Miao Y; Liang SY; Yu DY
Zhonghua Fu Chan Ke Za Zhi; 2019 Apr; 54(4):226-231. PubMed ID: 31006187
[No Abstract] [Full Text] [Related]
40. Cardiac Dysfunction in Duchenne Muscular Dystrophy Is Less Frequent in Patients With Mutations in the Dystrophin Dp116 Coding Region Than in Other Regions.
Yamamoto T; Awano H; Zhang Z; Sakuma M; Kitaaki S; Matsumoto M; Nagai M; Sato I; Imanishi T; Hayashi N; Matsuo M; Iijima K; Saegusa J
Circ Genom Precis Med; 2018 Jan; 11(1):e001782. PubMed ID: 29874176
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
