333 related articles for article (PubMed ID: 8139842)
21. Deletion analysis and clinical correlations in patients with Xp21 linked muscular dystrophy.
Ulgenalp A; Giray O; Bora E; Hizli T; Kurul S; Sağin-Saylam G; Karasoy H; Uran N; Dizdarer G; Tütüncüoğlu S; Dirik E; Ozkinay F; Erçal D
Turk J Pediatr; 2004; 46(4):333-8. PubMed ID: 15641267
[TBL] [Abstract][Full Text] [Related]
22. 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]
23. Characterization of genetic deletions in Becker muscular dystrophy using monoclonal antibodies against a deletion-prone region of dystrophin.
Le Thiet Thanh ; Nguyen Thi Man ; Hori S; Sewry CA; Dubowitz V; Morris GE
Am J Med Genet; 1995 Aug; 58(2):177-86. PubMed ID: 8533812
[TBL] [Abstract][Full Text] [Related]
24. Diagnosis and carrier detection in a Duchenne muscular dystrophy family by multiplex polymerase chain reaction and microsatellite analysis.
Jongpiputvanich S; Norapucsunton T; Mutirangura A
J Med Assoc Thai; 1996 Dec; 79 Suppl 1():S15-21. PubMed ID: 9071063
[TBL] [Abstract][Full Text] [Related]
25. Analysis of dystrophin gene deletions in patients from the Mexican population with Duchenne/Becker muscular dystrophy.
Coral-Vázquez R; Arenas D; Cisneros B; Peñaloza L; Kofman S; Salamanca F; Montañez C
Arch Med Res; 1993; 24(1):1-6. PubMed ID: 8292871
[TBL] [Abstract][Full Text] [Related]
26. [Deletion analysis of the dystrophin gene in patients with Duchenne's muscular dystrophy in Tajikistan].
Odinokova ON; Puzyrev VP; Radzhabaliev ShF; Rakhmonov RA
Genetika; 1996 Oct; 32(10):1392-5. PubMed ID: 9091412
[TBL] [Abstract][Full Text] [Related]
27. [Molecular genetics and problems found in genetic diagnosis of Duchenne Becker muscular dystrophy].
Takeshima Y; Matsuo M
Nihon Rinsho; 1997 Dec; 55(12):3120-5. PubMed ID: 9436421
[TBL] [Abstract][Full Text] [Related]
28. [Antepartum diagnosis of pseudohypertrophic muscular dystrophy using 14 sets of primers].
Wu Y
Zhonghua Yi Xue Za Zhi; 1993 Sep; 73(9):532-4, 574. PubMed ID: 8313195
[TBL] [Abstract][Full Text] [Related]
29. Multiplex PCR to detect the dystrophin gene deletion in Thai patients.
Mutirangura A; Jongpiputvanich S; Norapucsunton T; Theamboonlers A; Srivuthana S; Promchainant C; Tumwasorn S; Sueblinvong T
J Med Assoc Thai; 1995 Sep; 78(9):460-5. PubMed ID: 7561572
[TBL] [Abstract][Full Text] [Related]
30. [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]
31. [Mutation analysis and prenatal diagnosis of sporadic DMD/BMD families].
Zhu HY; Li J; Yang Y; Wu X; Zhu XY; Zhu RF; Zhang Y; Duan HL; Hu YL
Zhonghua Yi Xue Za Zhi; 2009 Jul; 89(25):1753-6. PubMed ID: 19862979
[TBL] [Abstract][Full Text] [Related]
32. [Prenatal diagnosis of Duchenne's muscular dystrophy fetus at risk].
Hua XY; Xu MH; Lin QD
Zhonghua Fu Chan Ke Za Zhi; 1994 Jul; 29(7):408-10, 445. PubMed ID: 8001417
[TBL] [Abstract][Full Text] [Related]
33. [Application of PCR technique in genetic diagnosis of Duchenne/Becker muscular dystrophy].
Liu YM; Feng ZC; Fang ZW
Di Yi Jun Yi Da Xue Xue Bao; 2002 Aug; 22(8):731-3. PubMed ID: 12376264
[TBL] [Abstract][Full Text] [Related]
34. Detection of gene deletions by PCR analysis in a Malaysian patient with Duchenne muscular dystrophy.
Lee MK; Manonmani V; Arahata K
Med J Malaysia; 1993 Mar; 48(1):46-50. PubMed ID: 8341171
[TBL] [Abstract][Full Text] [Related]
35. Screening of dystrophin gene deletions in Malaysian patients with Duchenne muscular dystrophy.
Marini M; Salmi AA; Watihayati MS; SMardziah MD; Zahri MK; Hoh BP; Ankathil R; Lai PS; Zilfalil BA
Med J Malaysia; 2008 Mar; 63(1):31-4. PubMed ID: 18935728
[TBL] [Abstract][Full Text] [Related]
36. [Detection of deletions by the amplification of exons (multiplex PCR) in Duchenne muscular dystrophy].
Claustres M; Kjellberg P; Desgeorges M; Bellet H; Sarda P; Bonnet H; Boileau C
J Genet Hum; 1989 Sep; 37(3):251-7. PubMed ID: 2625628
[TBL] [Abstract][Full Text] [Related]
37. [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]
38. Becker muscular dystrophy: detection of unusual disease courses by combined approach to dystrophin analysis.
Gold R; Kress W; Meurers B; Meng G; Reichmann H; Müller CR
Muscle Nerve; 1992 Feb; 15(2):214-8. PubMed ID: 1549142
[TBL] [Abstract][Full Text] [Related]
39. Detection of gene deletion in patients of Duchenne muscular dystrophy/Becker muscular dystrophy using polymerase chain reaction.
Sinha S; Pradhan S; Mittal RD; Mittal B
Indian J Med Res; 1992 Oct; 96():297-301. PubMed ID: 1459673
[TBL] [Abstract][Full Text] [Related]
40. [Preimplantation genetic diagnosis of Duchenne muscular dystrophy by single cell triplex PCR].
Wu YL; Wu LQ; Li YP; Liu DE; Zeng Q; Zhu HY; Pan Q; Liang DS; Hu H; Long ZG; Li J; Dai HP; Xia K; Xia JH
Zhong Nan Da Xue Xue Bao Yi Xue Ban; 2007 Apr; 32(2):246-51. PubMed ID: 17478931
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]