BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

313 related articles for article (PubMed ID: 8629100)

  • 1. Detection of DMD gene deletions in Thai children patients.
    Kamolsilp M; Paditaporn R; Noonai A; Wasant P
    Southeast Asian J Trop Med Public Health; 1995; 26 Suppl 1():172-4. PubMed ID: 8629100
    [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. [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]  

  • 4. 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]  

  • 5. Southern blot and PCR analyses of dystrophin gene deletions in Japanese patients with Duchenne muscular dystrophy.
    Nakajima T; Matsuo M; Nakamura H; Fujiwara Y
    Kobe J Med Sci; 1991 Feb; 37(1):21-33. PubMed ID: 1921260
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 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. Deletion screening of the Duchenne/Becker muscular dystrophy gene in Croatian population.
    Sertić J; Barisić N; Sostarko M; Brzović Z; Stavljenić-Rukavina A
    Coll Antropol; 1997 Jun; 21(1):151-6. PubMed ID: 9225508
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Are there ethnic differences in deletions in the dystrophin gene?
    Banerjee M; Verma IC
    Am J Med Genet; 1997 Jan; 68(2):152-7. PubMed ID: 9028449
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Comparative study on deletions of the dystrophin gene in three Asian populations.
    Lai PS; Takeshima Y; Adachi K; Van Tran K; Nguyen HT; Low PS; Matsuo M
    J Hum Genet; 2002; 47(10):552-5. PubMed ID: 12376747
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Studying dystrophin gene deletion in the northeast of China and applicating].
    Lu Y; Jin CL; Lin CK; Wu YY; Liu LY; Sun KL
    Yi Chuan Xue Bao; 2004 May; 31(5):449-53. PubMed ID: 15478603
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. 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]  

  • 15. [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]  

  • 16. [Rapid screening of the Duchenne muscular dystrophy gene deletion by two multiplex PCR].
    Ma S
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 1993 Feb; 15(1):74-8. PubMed ID: 8324844
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Molecular genetic and immunological analysis of dystrophin of a young patient with X-linked muscular dystrophy.
    Ikeya K; Saito K; Hayashi K; Tanaka H; Hagiwara Y; Yoshida M; Yamauchi A; Fukuyama Y; Ishiguro T; Eguchi C
    Am J Med Genet; 1992 Jun; 43(3):580-7. PubMed ID: 1605252
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Amplification of selected exons by polymerase chain reaction enables determination of the translational reading frame of dystrophin mRNA resulting from deletion mutations.
    Kitoh Y; Matsuo M; Nishio H; Nakamura H
    Kobe J Med Sci; 1994 Apr; 40(2):39-48. PubMed ID: 7823533
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Analysis of deletion mutations of the dystrophin gene by the multiplex polymerase chain reaction method in the diagnosis of Duchenne muscular dystrophy].
    Baranov Vs; Gorbunova VN; Malysheva OV; Krasil'nikov VV
    Mol Gen Mikrobiol Virusol; 1991 Sep; (9):13-5. PubMed ID: 1745268
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 16.