259 related articles for article (PubMed ID: 8173987)
21. Deletions in the dystrophin gene: analysis of Duchenne and Becker muscular dystrophy patients in Quebec.
Simard LR; Gingras F; Delvoye N; Vanasse M; Melançon SB; Labuda D
Hum Genet; 1992 Jun; 89(4):419-24. PubMed ID: 1618490
[TBL] [Abstract][Full Text] [Related]
22. Gene deletions in Japanese patients with Duchenne and Becker muscular dystrophy.
Asano J; Tomatsu S; Sukegawa K; Yamaguchi S; Ikedo Y; Minami R; Iida M; Nishimura M; Nakagawa M; Ohshiro M
Jinrui Idengaku Zasshi; 1990 Jun; 35(2):159-68. PubMed ID: 2398631
[TBL] [Abstract][Full Text] [Related]
23. [Analysis of deletion mutations of the dystrophin gene by the multiplex polymerase chain reaction method in the diagnosis of Duchenne muscular dystrophy].
Baranov Vs; Gorbunova VN; Malysheva OV; Krasil'nikov VV
Mol Gen Mikrobiol Virusol; 1991 Sep; (9):13-5. PubMed ID: 1745268
[TBL] [Abstract][Full Text] [Related]
24. [Analysis of deletions in the dystrophin gene in patients with Duchenne muscular dystrophy in the Bashkir Republic].
Grinchuk OV; Khidiiatova IM; Kiselev AV; Magzhanov RV; Khusnutdinova EK
Genetika; 1999 Apr; 35(4):551-5. PubMed ID: 10420280
[TBL] [Abstract][Full Text] [Related]
25. Clinical diagnosis of heterozygous dystrophin gene deletions by fluorescence in situ hybridization.
Rosenberg C; Navajas L; Vagenas DF; Bakker E; Vainzof M; Passos-Bueno MR; Takata RI; Van Ommen GJ; Zatz M; Den Dunnen JT
Neuromuscul Disord; 1998 Oct; 8(7):447-52. PubMed ID: 9829273
[TBL] [Abstract][Full Text] [Related]
26. Molecular-genetic study of Duchenne and Becker muscular dystrophies: deletion analyses of 45 Japanese patients and segregation analyses in their families with RFLPs based on the data from normal Japanese females.
Sugino S; Fujishita S; Kamimura N; Matsumoto T; Wapenaar MC; Deng HX; Shibuya N; Miike T; Niikawa N
Am J Med Genet; 1989 Dec; 34(4):555-61. PubMed ID: 2576185
[TBL] [Abstract][Full Text] [Related]
27. Apparent association of mental retardation and specific patterns of deletions screened with probes cf56a and cf23a in Duchenne muscular dystrophy.
Rapaport D; Passos-Bueno MR; Brandão L; Love D; Vainzof M; Zatz M
Am J Med Genet; 1991 Jun; 39(4):437-41. PubMed ID: 1877622
[TBL] [Abstract][Full Text] [Related]
28. Patterns of exon deletions in Duchenne and Becker muscular dystrophy.
Read AP; Mountford RC; Forrest SM; Kenwrick SJ; Davies KE; Harris R
Hum Genet; 1988 Oct; 80(2):152-6. PubMed ID: 3169738
[TBL] [Abstract][Full Text] [Related]
29. [Detection of extensive deletions and duplications in the dystrophin gene].
Fajkusová L; Kuhrová V; Hájek J; Fajkus J
Cas Lek Cesk; 1997 Mar; 136(5):148-50. PubMed ID: 9221188
[TBL] [Abstract][Full Text] [Related]
30. Gene-deletion and carrier detections, and prenatal diagnosis of Duchenne muscular dystrophy by analysis of the dystrophin gene amplified by polymerase chain reaction.
Fujishita S; Shibuya N; Niikawa N; Nagataki S
Jinrui Idengaku Zasshi; 1991 Dec; 36(4):317-24. PubMed ID: 1811098
[TBL] [Abstract][Full Text] [Related]
31. Molecular genetic analysis of 67 patients with Duchenne/Becker muscular dystrophy.
Niemann-Seyde S; Slomski R; Rininsland F; Ellermeyer U; Kwiatkowska J; Reiss J
Hum Genet; 1992; 90(1-2):65-70. PubMed ID: 1427789
[TBL] [Abstract][Full Text] [Related]
32. Screening of deletions in the dystrophin gene with the cDNA probes Cf23a, Cf56a, and Cf115.
Passos-Bueno MR; Rapaport D; Love D; Flint T; Bortolini ER; Zatz M; Davies KE
J Med Genet; 1990 Mar; 27(3):145-50. PubMed ID: 2182872
[TBL] [Abstract][Full Text] [Related]
33. Deletion analysis of the dystrophin gene in Duchenne and Becker muscular dystrophy patients: use in carrier diagnosis.
Kumari D; Mital A; Gupta M; Goyle S
Neurol India; 2003 Jun; 51(2):223-6. PubMed ID: 14571009
[TBL] [Abstract][Full Text] [Related]
34. Molecular and phenotypic analysis of patients with deletions within the deletion-rich region of the Duchenne muscular dystrophy (DMD) gene.
Gillard EF; Chamberlain JS; Murphy EG; Duff CL; Smith B; Burghes AH; Thompson MW; Sutherland J; Oss I; Bodrug SE
Am J Hum Genet; 1989 Oct; 45(4):507-20. PubMed ID: 2491010
[TBL] [Abstract][Full Text] [Related]
35. [Combining approach with multiplex PCR and MLPA to detect deletion and duplication in DMD patients, carriers, and prenatal diagnosis].
Li H; Ding J; Wang W; Chen Y; Lu W; Shao H; Wu BL
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Jun; 26(3):318-22. PubMed ID: 19504448
[TBL] [Abstract][Full Text] [Related]
36. Direct method for prenatal diagnosis and carrier detection in Duchenne/Becker muscular dystrophy using the entire dystrophin cDNA.
Darras BT; Koenig M; Kunkel LM; Francke U
Am J Med Genet; 1988 Mar; 29(3):713-26. PubMed ID: 2897793
[TBL] [Abstract][Full Text] [Related]
37. Deletion analysis of Duchenne muscular dystrophy.
Erdem H; Ayter S; Ozgüç M; Topçu M; Topaloğlu H; Renda Y
Turk J Pediatr; 1993; 35(1):15-21. PubMed ID: 8236513
[TBL] [Abstract][Full Text] [Related]
38. 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]
39. Gene deletions in X-linked muscular dystrophy.
Lindlöf M; Kiuru A; Kääriäinen H; Kalimo H; Lang H; Pihko H; Rapola J; Somer H; Somer M; Savontaus ML
Am J Hum Genet; 1989 Apr; 44(4):496-503. PubMed ID: 2929594
[TBL] [Abstract][Full Text] [Related]
40. Pattern of deletions of the dystrophin gene in Mexican Duchenne/Becker muscular dystrophy patients: the use of new designed primers for the analysis of the major deletion "hot spot" region.
Coral-Vazquez R; Arenas D; Cisneros B; Peñaloza L; Salamanca F; Kofman S; Mercado R; Montañez C
Am J Med Genet; 1997 Jun; 70(3):240-6. PubMed ID: 9188659
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]