BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

1279 related articles for article (PubMed ID: 18752307)

  • 1. 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]  

  • 2. Detection of exonic copy-number changes using a highly efficient oligonucleotide-based comparative genomic hybridization-array method.
    Saillour Y; Cossée M; Leturcq F; Vasson A; Beugnet C; Poirier K; Commere V; Sublemontier S; Viel M; Letourneur F; Barbot JC; Deburgrave N; Chelly J; Bienvenu T
    Hum Mutat; 2008 Sep; 29(9):1083-90. PubMed ID: 18683213
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Duchenne muscular dystrophy caused by a complex rearrangement between intron 43 of the DMD gene and chromosome 4.
    Baskin B; Gibson WT; Ray PN
    Neuromuscul Disord; 2011 Mar; 21(3):178-82. PubMed ID: 21134752
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [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]  

  • 5. Genetic diagnosis of Duchenne and Becker muscular dystrophy using next-generation sequencing technology: comprehensive mutational search in a single platform.
    Lim BC; Lee S; Shin JY; Kim JI; Hwang H; Kim KJ; Hwang YS; Seo JS; Chae JH
    J Med Genet; 2011 Nov; 48(11):731-6. PubMed ID: 21969337
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. 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]  

  • 8. Duplications in the DMD gene.
    White SJ; Aartsma-Rus A; Flanigan KM; Weiss RB; Kneppers AL; Lalic T; Janson AA; Ginjaar HB; Breuning MH; den Dunnen JT
    Hum Mutat; 2006 Sep; 27(9):938-45. PubMed ID: 16917894
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [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]  

  • 10. 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]  

  • 11. 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]  

  • 12. [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]  

  • 13. 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]  

  • 14. 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]  

  • 15. Microarray-based mutation detection in the dystrophin gene.
    Hegde MR; Chin EL; Mulle JG; Okou DT; Warren ST; Zwick ME
    Hum Mutat; 2008 Sep; 29(9):1091-9. PubMed ID: 18663755
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Detecting exon deletions and duplications of the DMD gene using Multiplex Ligation-dependent Probe Amplification (MLPA).
    Lai KK; Lo IF; Tong TM; Cheng LY; Lam ST
    Clin Biochem; 2006 Apr; 39(4):367-72. PubMed ID: 16413013
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. [Comparison and analysis of the molecular character of breakpoints in introns of deletion hotspots of dystrophin gene].
    Sheng WL; Chen JY; Pan SY; Zhang C; Liu ZL
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2003 Oct; 20(5):376-80. PubMed ID: 14556187
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 64.