These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

109 related articles for article (PubMed ID: 9339110)

  • 1. Correlation of laboratory and clinical findings with the location of Xp21 deletion in Duchenne muscular dystrophy.
    Taşdemir HA; Topaloğlu H; Dinçer P; Göğüş S; Kotiloğlu E; Ozdirim E; Yalaz K
    Turk J Pediatr; 1997; 39(3):317-24. PubMed ID: 9339110
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Molecular analysis of the Duchenne muscular dystrophy gene in patients with Becker muscular dystrophy presenting with dilated cardiomyopathy.
    Yoshida K; Ikeda S; Nakamura A; Kagoshima M; Takeda S; Shoji S; Yanagisawa N
    Muscle Nerve; 1993 Nov; 16(11):1161-6. PubMed ID: 8413368
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. Absence of correlation between utrophin localization and quantity and the clinical severity in Duchenne/Becker dystrophies.
    Vainzof M; Passos-Bueno MR; Man N; Zatz M
    Am J Med Genet; 1995 Sep; 58(4):305-9. PubMed ID: 8533838
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Screening of dystrophin gene deletions in Malaysian patients with Duchenne muscular dystrophy.
    Marini M; Salmi AA; Watihayati MS; SMardziah MD; Zahri MK; Hoh BP; Ankathil R; Lai PS; Zilfalil BA
    Med J Malaysia; 2008 Mar; 63(1):31-4. PubMed ID: 18935728
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Deletion analysis and clinical correlations in patients with Xp21 linked muscular dystrophy.
    Ulgenalp A; Giray O; Bora E; Hizli T; Kurul S; Sağin-Saylam G; Karasoy H; Uran N; Dizdarer G; Tütüncüoğlu S; Dirik E; Ozkinay F; Erçal D
    Turk J Pediatr; 2004; 46(4):333-8. PubMed ID: 15641267
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. [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]  

  • 10. [The distribution of deletions in the dystrophin gene in patients with Duchenne muscular dystrophy in Ukraine].
    Grishko VI; Maliarchuk SG; Livshits LA
    Tsitol Genet; 1993; 27(2):68-71. PubMed ID: 8212329
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [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]  

  • 12. 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]  

  • 13. Newly recognized exons induced by a splicing abnormality from an intronic mutation of the dystrophin gene resulting in Duchenne muscular dystrophy. Mutations in brief no. 213. Online.
    Ikezawa M; Nishino I; Goto Y; Miike T; Nonaka I
    Hum Mutat; 1999; 13(2):170. PubMed ID: 10094556
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Deletion analysis of Duchenne muscular dystrophy.
    Erdem H; Ayter S; Ozgüç M; Topçu M; Topaloğlu H; Renda Y
    Turk J Pediatr; 1993; 35(1):15-21. PubMed ID: 8236513
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Family study allows more optimistic prognosis and genetic counselling in a child with a deletion of exons 50-51 of the dystrophin gene].
    Lesca G; Testard H; Streichenberger N; Pelissier JF; Lestra C; Burel E; Jonveaux P; Michel-Calemard L
    Arch Pediatr; 2007 Mar; 14(3):262-5. PubMed ID: 17258443
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Cloning and sequencing of the junction fragment of dystrophin gene with exons 3 to 5 deletion].
    Zhong M; Pan SY; Lu BX; Jiang L; Li W
    Nan Fang Yi Ke Da Xue Xue Bao; 2006 Jun; 26(6):757-9. PubMed ID: 16793593
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Duchenne muscular dystrophy and myotonic dystrophy in the same patient.
    Dubrovsky AL; Taratuto AL; Sevlever G; Schultz M; Pegoraro E; Hoop RC; Hoffman EP
    Am J Med Genet; 1995 Jan; 55(3):342-8. PubMed ID: 7726234
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Asymptomatic Becker muscular dystrophy in a family with a multiexon deletion.
    Ferreiro V; Giliberto F; Muñiz GM; Francipane L; Marzese DM; Mampel A; Roqué M; Frechtel GD; Szijan I
    Muscle Nerve; 2009 Feb; 39(2):239-43. PubMed ID: 19012301
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Paternal inheritance or a de novo mutation in a Duchenne Muscular Dystrophy pedigree from South India.
    Purushottam M; Murthy AR; Shubha GN; Gayathri N; Nalini A
    J Neurol Sci; 2008 May; 268(1-2):179-82. PubMed ID: 18031759
    [TBL] [Abstract][Full Text] [Related]  

  • 20. More deletions in the 5' region than in the central region of the dystrophin gene were identified among Filipino Duchenne and Becker muscular dystrophy patients.
    Cutiongco EM; Padilla CD; Takenaka K; Yamasaki Y; Matsuo M; Nishio H
    Am J Med Genet; 1995 Nov; 59(2):266-7. PubMed ID: 8588598
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.