441 related articles for article (PubMed ID: 2576185)
1. 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]
2. 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]
3. DNA analysis of Duchenne and Becker muscular dystrophy using pERT87 genomic probes and dystrophin cDNA probes--establishing the optimum strategy for carrier diagnosis in the Japanese population.
Ubagai T; Katayama S
Jinrui Idengaku Zasshi; 1991 Sep; 36(3):211-27. PubMed ID: 1684391
[TBL] [Abstract][Full Text] [Related]
4. Gene-deletion and carrier detections, and prenatal diagnosis of Duchenne muscular dystrophy by analysis of the dystrophin gene amplified by polymerase chain reaction.
Fujishita S; Shibuya N; Niikawa N; Nagataki S
Jinrui Idengaku Zasshi; 1991 Dec; 36(4):317-24. PubMed ID: 1811098
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. 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]
8. 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]
9. 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]
10. 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]
11. [Molecular biology in genetic counseling of Duchenne and Becker myopathy].
Philip N; Voelckel MA; Girardot L; Lambert JC; Moncla A; Mattei JF; Giraud F
Pediatrie; 1992; 47(12):821-8. PubMed ID: 1338927
[TBL] [Abstract][Full Text] [Related]
12. Preferential deletion of exons in Duchenne and Becker muscular dystrophies.
Forrest SM; Cross GS; Speer A; Gardner-Medwin D; Burn J; Davies KE
Nature; 1987 Oct 15-21; 329(6140):638-40. PubMed ID: 2821406
[TBL] [Abstract][Full Text] [Related]
13. Germline mosaicism and Duchenne muscular dystrophy mutations.
Bakker E; Van Broeckhoven C; Bonten EJ; van de Vooren MJ; Veenema H; Van Hul W; Van Ommen GJ; Vandenberghe A; Pearson PL
Nature; 1987 Oct 8-14; 329(6139):554-6. PubMed ID: 2889144
[TBL] [Abstract][Full Text] [Related]
14. Possibilities and limitations of carrier diagnosis in families with Duchenne muscular dystrophy caused by deletions in the major hot spot region using pulsed-field gel electrophoresis.
Huschenbett J; Volz A; Pfeifer L; Speer A
Biomed Biochim Acta; 1991; 50(12):1205-12. PubMed ID: 1824538
[TBL] [Abstract][Full Text] [Related]
15. [Carrier detection and gene analysis in a Duchenne muscular dystrophy family].
Lu FM
Zhonghua Shen Jing Jing Shen Ke Za Zhi; 1990 Aug; 23(4):231-3, 255. PubMed ID: 1979269
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Identification of carriers of Duchenne muscular dystrophy: value of molecular analysis.
LeRoy BS; Uhrhammer NA; Steere KJ; Boehm CD; King RA; Rich SS; Williams PP; Smith SA; de Martinville B
Am J Med Genet; 1988 Nov; 31(3):709-21. PubMed ID: 2906525
[TBL] [Abstract][Full Text] [Related]
18. [Mutation analysis and prenatal diagnosis of sporadic DMD/BMD families].
Zhu HY; Li J; Yang Y; Wu X; Zhu XY; Zhu RF; Zhang Y; Duan HL; Hu YL
Zhonghua Yi Xue Za Zhi; 2009 Jul; 89(25):1753-6. PubMed ID: 19862979
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Analysis of deletions in DNA from patients with Becker and Duchenne muscular dystrophy.
Kunkel LM; Hejtmancik JF; Caskey CT; Speer A; Monaco AP; Middlesworth W; Colletti CA; Bertelson C; Müller U; Bresnan M; Shapiro F; Tantravahi U; Speer J; Latt SA; Bartlett R; Pericak-Vance MA; Roses AD; Thompson MW; Ray PN; Worton RG; Fischbeck KH; Gallano P; Coulon M; Duros C; Boue J; Junien C; Chelly J; Hamard G; Jeanpierre M; Lambert M; Kaplan JC; Emery A; Dorkins H; McGlade S; Davies KE; Boehm C; Arveiler B; Lemaire C; Morgan GJ; Denton MJ; Amos J; Bobrow M; Benham F; Boswinkel E; Cole C; Dubowitz V; Hart K; Hodgson S; Johnson L; Walker A; Roncuzzi L; Ferlini A; Nobile C; Romeo G; Wilcox DE; Affara NA; Ferguson-Smith MA; Lindolf M; Kaariainen H; de la Chapelle A; Ionasescu V; Searby C; Ionasescu R; Bakker E; van Ommen GJ; Pearson PL; Greenberg CR; Hamerton JL; Wrogemann K; Doherty RA; Polakowska R; Hyser C; Quirk S; Thomas N; Harper JF; Darras BT; Francke U
Nature; 1986 Jul 3-9; 322(6074):73-7. PubMed ID: 3014348
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]