BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

350 related articles for article (PubMed ID: 17680544)

  • 1. [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]  

  • 2. [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]  

  • 3. [Identification of deletion/duplication mutations in DMD gene by multiple ligation probe amplification and denaturing high-performance liquid chromatography].
    Shen BC; Zhang C; Sun XF; Li SY
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 2007 Feb; 29(1):83-6. PubMed ID: 17380674
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 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]  

  • 6. [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]  

  • 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. 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]  

  • 9. Identification of deletions and duplications of the DMD gene in affected males and carrier females by multiple ligation probe amplification (MLPA).
    Gatta V; Scarciolla O; Gaspari AR; Palka C; De Angelis MV; Di Muzio A; Guanciali-Franchi P; Calabrese G; Uncini A; Stuppia L
    Hum Genet; 2005 Jun; 117(1):92-8. PubMed ID: 15841391
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 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. 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]  

  • 13. [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]  

  • 14. 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]  

  • 15. 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]  

  • 16. Improved detection of deletions and duplications in the DMD gene using the multiplex ligation-dependent probe amplification (MLPA) method.
    Sansović I; Barišić I; Dumić K
    Biochem Genet; 2013 Apr; 51(3-4):189-201. PubMed ID: 23224783
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. MLPA based detection of mutations in the dystrophin gene of 180 Polish families with Duchenne/Becker muscular dystrophy.
    Zimowski JG; Massalska D; Holding M; Jadczak S; Fidziańska E; Lusakowska A; Kostera-Pruszczyk A; Kamińska A; Zaremba J
    Neurol Neurochir Pol; 2014; 48(6):416-22. PubMed ID: 25482253
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Identification of deletions and duplications in the Duchenne muscular dystrophy gene and female carrier status in western India using combined methods of multiplex polymerase chain reaction and multiplex ligation-dependent probe amplification.
    Dastur RS; Kachwala MY; Khadilkar SV; Hegde MR; Gaitonde PS
    Neurol India; 2011; 59(6):803-9. PubMed ID: 22234189
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Deletion and duplication screening in the DMD gene using MLPA.
    Lalic T; Vossen RH; Coffa J; Schouten JP; Guc-Scekic M; Radivojevic D; Djurisic M; Breuning MH; White SJ; den Dunnen JT
    Eur J Hum Genet; 2005 Nov; 13(11):1231-4. PubMed ID: 16030524
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 18.