216 related articles for article (PubMed ID: 19409785)
1. Rapid and cost effective detection of small mutations in the DMD gene by high resolution melting curve analysis.
Almomani R; van der Stoep N; Bakker E; den Dunnen JT; Breuning MH; Ginjaar IB
Neuromuscul Disord; 2009 Jun; 19(6):383-90. PubMed ID: 19409785
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. Protein- and mRNA-based phenotype-genotype correlations in DMD/BMD with point mutations and molecular basis for BMD with nonsense and frameshift mutations in the DMD gene.
Deburgrave N; Daoud F; Llense S; Barbot JC; Récan D; Peccate C; Burghes AH; Béroud C; Garcia L; Kaplan JC; Chelly J; Leturcq F
Hum Mutat; 2007 Feb; 28(2):183-95. PubMed ID: 17041906
[TBL] [Abstract][Full Text] [Related]
5. Novel mutations of dystrophin gene in DMD patients detected by rapid scanning in biplex exons DHPLC analysis.
Muscarella LA; Piemontese MR; Barbano R; Fazio A; Guarnieri V; Quattrone A; Zelante L
Biomol Eng; 2007 Jun; 24(2):231-6. PubMed ID: 17145200
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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]
8. Use of multiplex ligation-dependent probe amplification (MLPA) for Duchenne muscular dystrophy (DMD) gene mutation analysis.
Murugan S; Chandramohan A; Lakshmi BR
Indian J Med Res; 2010 Sep; 132():303-11. PubMed ID: 20847377
[TBL] [Abstract][Full Text] [Related]
9. [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]
10. [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]
11. Validation and comparison of two quantitative real-time PCR assays for direct detection of DMD/BMD carriers.
Hayat Nosaeid M; Mahdian R; Jamali S; Maryami F; Babashah S; Maryami F; Karimipoor M; Zeinali S
Clin Biochem; 2009 Aug; 42(12):1291-9. PubMed ID: 19439162
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. [Identification of disease-causing point mutations in DMD patients' dystrophin gene without large deletions/duplications].
Shen BC; Zhang C; Chen SL; Sun XF; Li SY; Yao XL; Wang SH; Lu XL
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2006 Aug; 23(4):392-6. PubMed ID: 16883524
[TBL] [Abstract][Full Text] [Related]
14. [Detection of genomic duplications and deletions of the DMD gene in affected males and female carriers by using mutiplex ligation-dependent probe amplification].
Shen BC; Zhang C; Sun XF; Zhang HM; Li SY
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Aug; 24(4):460-3. PubMed ID: 17680544
[TBL] [Abstract][Full Text] [Related]
15. [Detection of micro mutation in dystrophin gene of DMD female carrier].
Miyamoto A; Taguchi K; Hieda S; Kawamura M; Fukuchi K; Gomi K
Rinsho Byori; 2004 Jun; 52(6):493-9. PubMed ID: 15283161
[TBL] [Abstract][Full Text] [Related]
16. Simultaneous mutation scanning for gross deletions, duplications and point mutations in the DMD gene.
Ashton EJ; Yau SC; Deans ZC; Abbs SJ
Eur J Hum Genet; 2008 Jan; 16(1):53-61. PubMed ID: 17726484
[TBL] [Abstract][Full Text] [Related]
17. [From gene to disease; the dystrophin gene involved in Duchenne and Becker muscular dystrophy].
den Dunnen JT; de Visser M; Bakker E
Ned Tijdschr Geneeskd; 2002 Feb; 146(8):364-7. PubMed ID: 11887623
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. 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]
20. Rapid prenatal diagnosis of Duchenne muscular dystrophy with gene duplications by ion-pair reversed-phase high-performance liquid chromatography coupled with competitive multiplex polymerase chain reaction strategy.
Huang WY; Hung CC; Lee CN; Su YN; Chen CP
Prenat Diagn; 2007 Jul; 27(7):653-6. PubMed ID: 17385798
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]