112 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]