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.
2. X;autosome translocations in females with Duchenne or Becker muscular dystrophy. Dubowitz V Nature; 1986 Jul 17-23; 322(6076):291-2. PubMed ID: 3461282 [No Abstract] [Full Text] [Related]
3. One family of benign X-linked pseudohypertrophic muscular dystrophy of early onset. Itoga E; Kito S Hiroshima J Med Sci; 1984 Sep; 33(3):303-10. PubMed ID: 6542554 [No Abstract] [Full Text] [Related]
4. [The molecular principles of Duchenne and Becker muscular dystrophy and their genetic diagnosis]. Speer A; Davies KE; Hanke R; Grade K; Spiegler AW; Herrmann FH; Szibor R; Wulff K; Sommer D; Metzke H Z Arztl Fortbild (Jena); 1989; 83(3):117-20. PubMed ID: 2655303 [No Abstract] [Full Text] [Related]
5. [Clinical polymorphism and genetic heterogeneity in Duchenne's progressive muscular dystrophy in girls (a review)]. Zavadenko NN; Temin PA; Malygina NA Zh Nevropatol Psikhiatr Im S S Korsakova; 1988; 88(11):123-6. PubMed ID: 3066079 [No Abstract] [Full Text] [Related]
6. [Gene deletion analysis in molecular diagnosis of Duchenne-Becker muscular dystrophy]. Endreffy E; László A; Kálmán M; Krenács T; Raskó I Orv Hetil; 1994 Feb; 135(8):399-403. PubMed ID: 8139842 [TBL] [Abstract][Full Text] [Related]
7. [Updates in muscular dystrophies]. Erazo-Torricelli R Rev Neurol; 2004 Nov 1-15; 39(9):860-71. PubMed ID: 15543503 [TBL] [Abstract][Full Text] [Related]
8. The muscular dystrophies. Bushby KM Baillieres Clin Neurol; 1994 Aug; 3(2):407-30. PubMed ID: 7952855 [TBL] [Abstract][Full Text] [Related]
9. Interrelationship between gene, its product and phenotype in Duchenne and Becker muscular dystrophy. Hausmanowa-Petrusewicz I; Zaremba J; Fidziańska A; Zimowski J; Bisko M; Badurska B; Fidziańska E; Lusakowska A; Borkowska J Acta Neurobiol Exp (Wars); 1993; 53(1):297-303. PubMed ID: 8317263 [TBL] [Abstract][Full Text] [Related]
10. Comparative analysis between Duchenne and Becker types muscular dystrophy. Ishpekova B; Milanov I; Christova LG; Alexandrov AS Electromyogr Clin Neurophysiol; 1999; 39(5):315-8. PubMed ID: 10422002 [TBL] [Abstract][Full Text] [Related]
12. [Correlation between electroretinographic findings, clinical phenotypic and genotypic analysis in Duchenne and Becker muscular dystrophy]. Yang Y; Zhang C; Sheng W; Pan S; Wu D; Jiang F Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2001 Feb; 18(1):32-4. PubMed ID: 11172639 [TBL] [Abstract][Full Text] [Related]
13. Absence of correlation between skewed X inactivation in blood and serum creatine-kinase levels in Duchenne/Becker female carriers. Sumita DR; Vainzof M; Campiotto S; Cerqueira AM; Cánovas M; Otto PA; Passos-Bueno MR; Zatz M Am J Med Genet; 1998 Dec; 80(4):356-61. PubMed ID: 9856563 [TBL] [Abstract][Full Text] [Related]
14. [Symposium II. Genetic and clinical types of muscular dystrophy]. Jinrui Idengaku Zasshi; 1974 Jun; 19(1):39-48. PubMed ID: 4476828 [No Abstract] [Full Text] [Related]
15. Muscular dystrophy (a clinical analysis of 126 cases). Mondkar VP; Bhabha SK J Postgrad Med; 1984 Oct; 30(4):224-8. PubMed ID: 6527309 [No Abstract] [Full Text] [Related]
16. Two families with late onset pseudohypertrophic muscular dystrophy (Becker type). Lee WL; Wong HB J Singapore Paediatr Soc; 1981; 23(3-4):159-63. PubMed ID: 7052857 [No Abstract] [Full Text] [Related]
17. [Muscular dystrophy of the Becker type]. Carbajal-Rodríguez L; de Quevedo JJ; Loredo-Abdalá A; Villaseñor-Zepeda J Bol Med Hosp Infant Mex; 1988 Sep; 45(9):605-9. PubMed ID: 3190853 [No Abstract] [Full Text] [Related]