165 related articles for article (PubMed ID: 10465346)
1. Detection of gene deletions in Chinese patients with Duchenne/Becker muscular dystrophy using CDNA probes and the polymerase chain reaction method.
Yuge L; Hui L; Bingdi X
Life Sci; 1999; 65(9):863-9. PubMed ID: 10465346
[TBL] [Abstract][Full Text] [Related]
2. Molecular deletion patterns in families from southern France with Duchenne/Becker muscular dystrophies.
Claustres M; Tuffery S; Chevron MP; Jozelon MP; Martinez P; Echenne B; Demaille J
Hum Genet; 1991 Dec; 88(2):179-84. PubMed ID: 1684565
[TBL] [Abstract][Full Text] [Related]
3. Molecular deletion patterns in Turkish Duchenne and Becker muscular dystrophy patients.
Dinçer P; Topaloğlu H; Ayter S; Ozgüç M; Taşdemir HA; Renda Y
Brain Dev; 1996; 18(2):91-4. PubMed ID: 8733896
[TBL] [Abstract][Full Text] [Related]
4. Correlation of clinical and deletion data in Duchenne and Becker muscular dystrophy, with special reference to mental ability.
Hodgson SV; Abbs S; Clark S; Manzur A; Heckmatt JZ; Dubowitz V; Bobrow M
Neuromuscul Disord; 1992; 2(4):269-76. PubMed ID: 1483053
[TBL] [Abstract][Full Text] [Related]
5. Deletion patterns in Argentine patients with Duchenne and Becker muscular dystrophy.
Baranzini SE; Giliberto F; Herrera M; Bernath V; Barreiro C; Garcia Erro M; Grippo J; Szijan I
Neurol Res; 1998 Jul; 20(5):409-414. PubMed ID: 9664586
[TBL] [Abstract][Full Text] [Related]
6. [Genetic analysis of 60 Duchenne muscular dystrophy (DMD) or Becker muscular dystrophy (BMD) patients using dystrophin cDNA].
Zhang J
Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 1993 Dec; 15(6):399-404. PubMed ID: 8082248
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. [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]
9. [Analysis of deletions in the dystrophin gene in patients with Duchenne muscular dystrophy in the Bashkir Republic].
Grinchuk OV; Khidiiatova IM; Kiselev AV; Magzhanov RV; Khusnutdinova EK
Genetika; 1999 Apr; 35(4):551-5. PubMed ID: 10420280
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Molecular and phenotypic analysis of patients with deletions within the deletion-rich region of the Duchenne muscular dystrophy (DMD) gene.
Gillard EF; Chamberlain JS; Murphy EG; Duff CL; Smith B; Burghes AH; Thompson MW; Sutherland J; Oss I; Bodrug SE
Am J Hum Genet; 1989 Oct; 45(4):507-20. PubMed ID: 2491010
[TBL] [Abstract][Full Text] [Related]
12. Deletions in the dystrophin gene: analysis of Duchenne and Becker muscular dystrophy patients in Quebec.
Simard LR; Gingras F; Delvoye N; Vanasse M; Melançon SB; Labuda D
Hum Genet; 1992 Jun; 89(4):419-24. PubMed ID: 1618490
[TBL] [Abstract][Full Text] [Related]
13. Characterization of translational frame exception patients in Duchenne/Becker muscular dystrophy.
Winnard AV; Klein CJ; Coovert DD; Prior T; Papp A; Snyder P; Bulman DE; Ray PN; McAndrew P; King W
Hum Mol Genet; 1993 Jun; 2(6):737-44. PubMed ID: 8353493
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. [Carrier detection in families affected by Duchenne/Becker muscular dystrophy].
Pikó H; Nagy B; Balog J; Bán Z; Herczegfalvi A; Karcagi V
Orv Hetil; 2007 Dec; 148(51):2403-9. PubMed ID: 18055393
[TBL] [Abstract][Full Text] [Related]
16. Detection of 98% of DMD/BMD gene deletions by polymerase chain reaction.
Beggs AH; Koenig M; Boyce FM; Kunkel LM
Hum Genet; 1990 Nov; 86(1):45-8. PubMed ID: 2253937
[TBL] [Abstract][Full Text] [Related]
17. Diagnosis of Duchenne and Becker muscular dystrophies by polymerase chain reaction. A multicenter study.
Chamberlain JS; Chamberlain JR; Fenwick RG; Ward PA; Caskey CT; Dimnik LS; Bech-Hansen NT; Hoar DI; Richards S; Covone AE; Govanni R; Abbs S; Bentley DR; Bobrow M; Rysiecki G; Ray PN; Boileau C; Junien C; Boehm C; Venne VL; Fujmura FK; Spiga I; Ferrari M; Tedeschi S; Bakker E; Kneppers AL; van Ommen GJ; Jain K; Spector E; Crandall B; Kiuru A; Savontaus ML; Caskey CT; Chamberlain JS; Chamberlain JR; Rysiecki G
JAMA; 1992 May; 267(19):2609-15. PubMed ID: 1573747
[TBL] [Abstract][Full Text] [Related]
18. Deletion patterns of Duchenne and Becker muscular dystrophies in Greece.
Florentin L; Mavrou A; Kekou K; Metaxotou C
J Med Genet; 1995 Jan; 32(1):48-51. PubMed ID: 7897627
[TBL] [Abstract][Full Text] [Related]
19. Distribution of dystrophin gene deletions in a Chinese population.
Li Y; Liu Z; OuYang S; Zhu Y; Wang L; Wu J
J Int Med Res; 2016 Feb; 44(1):99-108. PubMed ID: 26786758
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
