These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
268 related articles for article (PubMed ID: 9061750)
1. Prenatal diagnosis of Duchenne and Becker muscular dystrophy. Abbs S Prenat Diagn; 1996 Dec; 16(13):1187-98. PubMed ID: 9061750 [TBL] [Abstract][Full Text] [Related]
2. DNA diagnostic tests in Xp21 dystrophy families for prenatal diagnosis. Dinçer P; Topaloğlu H; Ayter S Turk J Pediatr; 1998; 40(3):347-55. PubMed ID: 9763898 [TBL] [Abstract][Full Text] [Related]
3. Molecular diagnosis of Duchenne muscular dystrophy by use of a conformational polymorphism in the absence of DNA from an affected boy. Tuffery S; Moine P; Sarda P; Lefort G; Boulot P; Demaille J; Claustres M Genet Couns; 1994; 5(2):183-5. PubMed ID: 7917130 [TBL] [Abstract][Full Text] [Related]
4. 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]
5. [Genotypic diagnosis of Duchenne and Becker muscular dystrophies]. Tuffery-Giraud S; Chambert S; Demaille J; Claustres M Ann Biol Clin (Paris); 1999; 57(4):417-26. PubMed ID: 10432364 [TBL] [Abstract][Full Text] [Related]
6. Genetic counseling of isolated carriers of Duchenne muscular dystrophy. Hoffman EP; Pegoraro E; Scacheri P; Burns RG; Taber JW; Weiss L; Spiro A; Blattner P Am J Med Genet; 1996 Jun; 63(4):573-80. PubMed ID: 8826437 [TBL] [Abstract][Full Text] [Related]
7. Experience and strategy for the molecular testing of Duchenne muscular dystrophy. Prior TW; Bridgeman SJ J Mol Diagn; 2005 Aug; 7(3):317-26. PubMed ID: 16049303 [TBL] [Abstract][Full Text] [Related]
8. [DNA diagnosis of Duchenne muscular dystrophy]. Matsumoto T No To Shinkei; 1991 May; 43(5):421-8. PubMed ID: 1680358 [No Abstract] [Full Text] [Related]
9. [Prenatal diagnosis of Duchenne muscular dystrophy using DNA RFLP analysis]. Zeng YT Zhonghua Yi Xue Za Zhi; 1988 Oct; 68(10):565-7, 38. PubMed ID: 2907413 [No Abstract] [Full Text] [Related]
10. DNA analysis and genetic counselling in Duchenne muscular dystrophy. Gardner RJ; Wilson SJ; Wilkins RJ N Z Med J; 1988 Jul; 101(849):455-7. PubMed ID: 3399183 [TBL] [Abstract][Full Text] [Related]
11. 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]
12. Rapid prenatal diagnosis of Duchenne muscular dystrophy with gene duplications by ion-pair reversed-phase high-performance liquid chromatography coupled with competitive multiplex polymerase chain reaction strategy. Huang WY; Hung CC; Lee CN; Su YN; Chen CP Prenat Diagn; 2007 Jul; 27(7):653-6. PubMed ID: 17385798 [TBL] [Abstract][Full Text] [Related]
13. ELISA quantitation of dystrophin for the diagnosis of Duchenne and Becker muscular dystrophies. Byers TJ; Neumann PE; Beggs AH; Kunkel LM Neurology; 1992 Mar; 42(3 Pt 1):570-6. PubMed ID: 1549217 [TBL] [Abstract][Full Text] [Related]
14. [Use of CA repeat polymorphism in direct and indirect diagnosis of Duchenne and Becker muscular dystrophy]. Musová Z; Mat'oska V; Krejcová S; Bóday A Cas Lek Cesk; 1997 Feb; 136(3):90-4. PubMed ID: 9221176 [TBL] [Abstract][Full Text] [Related]
16. Carrier detection by microsatellite analysis of Duchenne/Becker muscular dystrophy in Hungarian families. Bachrati CZ; Somodi Z; Endreffy E; Kalmár T; Raskó I Ann Hum Genet; 1998 Nov; 62(Pt 6):511-20. PubMed ID: 10363129 [TBL] [Abstract][Full Text] [Related]
17. Detection of a novel dystrophin gene mutation through carrier analysis performed during prenatal diagnosis in a case with intragenic recombination. Percesepe A; Ferrari M; Coviello D; Zanussi M; Castagni M; Neri I; Travi M; Forabosco A; Tedeschi S Prenat Diagn; 2005 Nov; 25(11):1011-4. PubMed ID: 16231306 [TBL] [Abstract][Full Text] [Related]
18. The clinical and molecular genetic approach to Duchenne and Becker muscular dystrophy: an updated protocol. van Essen AJ; Kneppers AL; van der Hout AH; Scheffer H; Ginjaar IB; ten Kate LP; van Ommen GJ; Buys CH; Bakker E J Med Genet; 1997 Oct; 34(10):805-12. PubMed ID: 9350811 [TBL] [Abstract][Full Text] [Related]
20. [Dystrophin and dystrophin-associated proteins. Their evaluation at the neuromuscular pathology laboratory]. Navarro C Rev Neurol; 1999 Jan 16-31; 28(2):154-8. PubMed ID: 10101784 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]