125 related articles for article (PubMed ID: 1893667)
1. [Two long-living brothers of dystrophin-related muscular dystrophy with an in-frame deletion of exon 3 of the dystrophin gene--clinical features and diagnosis].
Matsumura K; Imoto N
Rinsho Shinkeigaku; 1991 Mar; 31(3):286-90. PubMed ID: 1893667
[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. [Molecular genetics and problems found in genetic diagnosis of Duchenne Becker muscular dystrophy].
Takeshima Y; Matsuo M
Nihon Rinsho; 1997 Dec; 55(12):3120-5. PubMed ID: 9436421
[TBL] [Abstract][Full Text] [Related]
4. [From gene to disease; the dystrophin gene involved in Duchenne and Becker muscular dystrophy].
den Dunnen JT; de Visser M; Bakker E
Ned Tijdschr Geneeskd; 2002 Feb; 146(8):364-7. PubMed ID: 11887623
[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. Follow-up of three patients with a large in-frame deletion of exons 45-55 in the Duchenne muscular dystrophy (DMD) gene.
Nakamura A; Yoshida K; Fukushima K; Ueda H; Urasawa N; Koyama J; Yazaki Y; Yazaki M; Sakai T; Haruta S; Takeda S; Ikeda S
J Clin Neurosci; 2008 Jul; 15(7):757-63. PubMed ID: 18261911
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. [Manifesting carriers of Duchenne muscular dystrophy over two generations].
Itagaki Y; Saida K; Nishitani H; Matsuo M; Nishio H
Rinsho Shinkeigaku; 1993 Apr; 33(4):377-81. PubMed ID: 8103723
[TBL] [Abstract][Full Text] [Related]
9. Becker muscular dystrophy: detection of unusual disease courses by combined approach to dystrophin analysis.
Gold R; Kress W; Meurers B; Meng G; Reichmann H; Müller CR
Muscle Nerve; 1992 Feb; 15(2):214-8. PubMed ID: 1549142
[TBL] [Abstract][Full Text] [Related]
10. Large in-frame deletions of the rod-shaped domain of the dystrophin gene resulting in severe phenotype.
Nevo Y; Muntoni F; Sewry C; Legum C; Kutai M; Harel S; Dubowitz V
Isr Med Assoc J; 2003 Feb; 5(2):94-7. PubMed ID: 12674656
[TBL] [Abstract][Full Text] [Related]
11. Characterization of deletions in the dystrophin gene giving mild phenotypes.
Love DR; Flint TJ; Marsden RF; Bloomfield JF; Daniels RJ; Forrest SM; Gabrielli O; Giorgi P; Novelli G; Davies KE
Am J Med Genet; 1990 Sep; 37(1):136-42. PubMed ID: 2240031
[TBL] [Abstract][Full Text] [Related]
12. Gene deletions in Japanese patients with Duchenne and Becker muscular dystrophy.
Asano J; Tomatsu S; Sukegawa K; Yamaguchi S; Ikedo Y; Minami R; Iida M; Nishimura M; Nakagawa M; Ohshiro M
Jinrui Idengaku Zasshi; 1990 Jun; 35(2):159-68. PubMed ID: 2398631
[TBL] [Abstract][Full Text] [Related]
13. Deletion analysis of the dystrophin gene in Duchenne and Becker muscular dystrophy patients: use in carrier diagnosis.
Kumari D; Mital A; Gupta M; Goyle S
Neurol India; 2003 Jun; 51(2):223-6. PubMed ID: 14571009
[TBL] [Abstract][Full Text] [Related]
14. Re-evaluation of reading frame-shift hypothesis in Duchenne and Becker muscular dystrophy.
Pandey GS; Kesari A; Mukherjee M; Mittal RD; Mittal B
Neurol India; 2003 Sep; 51(3):367-9. PubMed ID: 14652441
[TBL] [Abstract][Full Text] [Related]
15. Direct method for prenatal diagnosis and carrier detection in Duchenne/Becker muscular dystrophy using the entire dystrophin cDNA.
Darras BT; Koenig M; Kunkel LM; Francke U
Am J Med Genet; 1988 Mar; 29(3):713-26. PubMed ID: 2897793
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Identification of a point mutation and germinal mosaicism in a Duchenne muscular dystrophy family.
Wilton SD; Chandler DC; Kakulas BA; Laing NG
Hum Mutat; 1994; 3(2):133-40. PubMed ID: 8199594
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. 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]
20. 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]
[Next] [New Search]