645 related articles for article (PubMed ID: 16608904)
1. PGD for dystrophin gene deletions using fluorescence in situ hybridization.
Malmgren H; White I; Johansson S; Levkov L; Iwarsson E; Fridström M; Blennow E
Mol Hum Reprod; 2006 May; 12(5):353-6. PubMed ID: 16608904
[TBL] [Abstract][Full Text] [Related]
2. Identification of female carriers for Duchenne and Becker muscular dystrophies using a FISH-based approach.
Ligon AH; Kashork CD; Richards CS; Shaffer LG
Eur J Hum Genet; 2000 Apr; 8(4):293-8. PubMed ID: 10854113
[TBL] [Abstract][Full Text] [Related]
3. [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]
4. [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]
5. Preimplantation genetic diagnosis for Duchenne muscular dystrophy by multiple displacement amplification.
Ren Z; Zeng HT; Xu YW; Zhuang GL; Deng J; Zhang C; Zhou CQ
Fertil Steril; 2009 Feb; 91(2):359-64. PubMed ID: 18359022
[TBL] [Abstract][Full Text] [Related]
6. Preimplantation genetic diagnosis (PGD) for Duchenne muscular dystrophy (DMD) by triplex-nested PCR.
Malcov M; Ben-Yosef D; Schwartz T; Mey-Raz N; Azem F; Lessing JB; Amit A; Yaron Y
Prenat Diagn; 2005 Dec; 25(13):1200-5. PubMed ID: 16353285
[TBL] [Abstract][Full Text] [Related]
7. Relatively low proportion of dystrophin gene deletions in Israeli Duchenne and Becker muscular dystrophy patients.
Shomrat R; Gluck E; Legum C; Shiloh Y
Am J Med Genet; 1994 Feb; 49(4):369-73. PubMed ID: 8160727
[TBL] [Abstract][Full Text] [Related]
8. [Detection of the gene-deleted female carriers of Duchenne/Becker muscular dystrophy using a fluorescent in situ hybridization based method].
Qi QW; Sun NH; Hao N
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2003 Aug; 20(4):350-2. PubMed ID: 12903051
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Deletion mutations in the dystrophin gene of Saudi patients with Duchenne and Becker muscular dystrophy.
Al-Jumah M; Majumdar R; Al-Rajeh S; Chaves-Carballo E; Salih MM; Awada A; Al-Shahwan S; Al-Uthaim S
Saudi Med J; 2002 Dec; 23(12):1478-82. PubMed ID: 12518196
[TBL] [Abstract][Full Text] [Related]
11. MLPA analysis/complete sequencing of the DMD gene in a group of Bulgarian Duchenne/Becker muscular dystrophy patients.
Todorova A; Todorov T; Georgieva B; Lukova M; Guergueltcheva V; Kremensky I; Mitev V
Neuromuscul Disord; 2008 Aug; 18(8):667-70. PubMed ID: 18653336
[TBL] [Abstract][Full Text] [Related]
12. Molecular diagnosis of Duchenne/Becker muscular dystrophy: enhanced detection of dystrophin gene rearrangements by oligonucleotide array-comparative genomic hybridization.
del Gaudio D; Yang Y; Boggs BA; Schmitt ES; Lee JA; Sahoo T; Pham HT; Wiszniewska J; Chinault AC; Beaudet AL; Eng CM
Hum Mutat; 2008 Sep; 29(9):1100-7. PubMed ID: 18752307
[TBL] [Abstract][Full Text] [Related]
13. [Gene deletion analysis in molecular diagnosis of Duchenne-Becker muscular dystrophy].
Endreffy E; László A; Kálmán M; Krenács T; Raskó I
Orv Hetil; 1994 Feb; 135(8):399-403. PubMed ID: 8139842
[TBL] [Abstract][Full Text] [Related]
14. DGGE-based whole-gene mutation scanning of the dystrophin gene in Duchenne and Becker muscular dystrophy patients.
Hofstra RM; Mulder IM; Vossen R; de Koning-Gans PA; Kraak M; Ginjaar IB; van der Hout AH; Bakker E; Buys CH; van Ommen GJ; van Essen AJ; den Dunnen JT
Hum Mutat; 2004 Jan; 23(1):57-66. PubMed ID: 14695533
[TBL] [Abstract][Full Text] [Related]
15. Mutation and haplotype analysis for Duchenne muscular dystrophy by single cell multiple displacement amplification.
Ren Z; Zhou C; Xu Y; Deng J; Zeng H; Zeng Y
Mol Hum Reprod; 2007 Jun; 13(6):431-6. PubMed ID: 17439955
[TBL] [Abstract][Full Text] [Related]
16. Dystrophin gene analysis in Hungarian Duchenne/Becker muscular dystrophy families - detection of carrier status in symptomatic and asymptomatic female relatives.
Pikó H; Vancsó V; Nagy B; Bán Z; Herczegfalvi A; Karcagi V
Neuromuscul Disord; 2009 Feb; 19(2):108-12. PubMed ID: 19084397
[TBL] [Abstract][Full Text] [Related]
17. [Genotypic diagnosis of Duchenne and Becker muscular dystrophies].
Tuffery-Giraud S; Chambert S; Demaille J; Claustres M
Ann Biol Clin (Paris); 1999; 57(4):417-26. PubMed ID: 10432364
[TBL] [Abstract][Full Text] [Related]
18. [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]
19. 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]
20. Multiexon skipping leading to an artificial DMD protein lacking amino acids from exons 45 through 55 could rescue up to 63% of patients with Duchenne muscular dystrophy.
Béroud C; Tuffery-Giraud S; Matsuo M; Hamroun D; Humbertclaude V; Monnier N; Moizard MP; Voelckel MA; Calemard LM; Boisseau P; Blayau M; Philippe C; Cossée M; Pagès M; Rivier F; Danos O; Garcia L; Claustres M
Hum Mutat; 2007 Feb; 28(2):196-202. PubMed ID: 17041910
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
