307 related articles for article (PubMed ID: 1898245)
1. Genetic analysis of the Duchenne muscular dystrophy gene.
Prior TW
Arch Pathol Lab Med; 1991 Oct; 115(10):984-90. PubMed ID: 1898245
[TBL] [Abstract][Full Text] [Related]
2. Potential pitfalls in using DNA probes to counsel Duchenne and Becker muscular dystrophy families.
Shi YJ; Fischbeck KH; Ritter A
Chin Med J (Engl); 1992 Jun; 105(6):469-75. PubMed ID: 1451547
[TBL] [Abstract][Full Text] [Related]
3. Experience with DNA analysis in Duchenne and Becker muscular dystrophy families in NSW.
Morgan G; Donald JA; Chen J; Serravalle S; Colley P; Denton MJ
Aust Paediatr J; 1988; 24 Suppl 1():98-9. PubMed ID: 3202741
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Molecular-genetic study of Duchenne and Becker muscular dystrophies: deletion analyses of 45 Japanese patients and segregation analyses in their families with RFLPs based on the data from normal Japanese females.
Sugino S; Fujishita S; Kamimura N; Matsumoto T; Wapenaar MC; Deng HX; Shibuya N; Miike T; Niikawa N
Am J Med Genet; 1989 Dec; 34(4):555-61. PubMed ID: 2576185
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Deletion analysis of Duchenne muscular dystrophy using cDNA probes and multiplex PCR.
Radosavljević D; Todorović D; Crkvenjakov R
Neurol Croat; 1991; 40(3):157-64. PubMed ID: 1681950
[TBL] [Abstract][Full Text] [Related]
8. Application of DNA probes to carrier detection and prenatal diagnosis of Duchenne (and Becker) muscular dystrophy.
Mulley JC; Gedeon AK; Haan EA; Sheffield LJ; White SJ; Bates LJ; Robertson EF; Sutherland GR
Aust Paediatr J; 1988; 24 Suppl 1():92-7. PubMed ID: 3202740
[TBL] [Abstract][Full Text] [Related]
9. Update on the molecular genetics of Duchenne muscular dystrophy.
Siddique T; Bartlett R; Pericak-Vance M; Yamaoka L; Koh J; Chen J; Hung WY; Kandt R; Roses AD
Aust Paediatr J; 1988; 24 Suppl 1():9-14. PubMed ID: 3060079
[TBL] [Abstract][Full Text] [Related]
10. Molecular deletion patterns in Duchenne muscular dystrophy patients.
Lucotte G; David F; Levy C
Ann Genet; 1989; 32(4):214-9. PubMed ID: 2610487
[TBL] [Abstract][Full Text] [Related]
11. Carrier detection by DNA analysis in Duchenne muscular dystrophy families.
Battaloğlu E; Telatar M; Deymeer F; Serdaroğlu P; Ozdemir C; Kuseyri F; Apak MY; Tolun A
Turk J Pediatr; 1992; 34(2):79-92. PubMed ID: 1440954
[TBL] [Abstract][Full Text] [Related]
12. [DNA-diagnosis of carriers of the Duchenne muscular dystrophy gene].
Evgrafov OV; Poliakov AV; Zaĭtseva SP; Malygina NA; Badalian LO; Makarov VB
Mol Gen Mikrobiol Virusol; 1990 Dec; (12):15-7. PubMed ID: 2084541
[TBL] [Abstract][Full Text] [Related]
13. Perspectives and molecular diagnosis of Duchenne and Becker muscular dystrophies.
Prior TW
Clin Lab Med; 1995 Dec; 15(4):927-41. PubMed ID: 8838231
[TBL] [Abstract][Full Text] [Related]
14. Genetic counseling issues in the use of DNA analysis for Duchenne/Becker muscular dystrophy.
Cortada JM; Milsark I; Richards CS
Birth Defects Orig Artic Ser; 1990; 26(3):231-7. PubMed ID: 2092850
[No Abstract] [Full Text] [Related]
15. Molecular genetics in muscular dystrophy research: revolutionary progress.
Stedman H; Sarkar S
Muscle Nerve; 1988 Jul; 11(7):683-93. PubMed ID: 3043215
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Carrier detection and prenatal diagnosis of Duchenne/Becker muscular dystrophy (D/BMD) by DNA-analysis.
Bakker E; Bonten EJ; den Dunnen JT; Veenema H; Grootscholten PM; van Ommen GJ; Pearson PL
Prog Clin Biol Res; 1989; 306():51-67. PubMed ID: 2662213
[No Abstract] [Full Text] [Related]
18. The muscular dystrophies.
Bushby KM
Baillieres Clin Neurol; 1994 Aug; 3(2):407-30. PubMed ID: 7952855
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Direct detection of more than 50% of the Duchenne muscular dystrophy mutations by field inversion gels.
den Dunnen JT; Bakker E; Breteler EG; Pearson PL; van Ommen GJ
Nature; 1987 Oct 15-21; 329(6140):640-2. PubMed ID: 2889148
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]