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.
32. [Pseudohypertrophic proximal progressive muscular dystrophy with a malignant course manifesting itself in adolescence]. Badalian LO; Temin PA; Saidbegov DG; Nikitin MV; Arkhipov BA Zh Nevropatol Psikhiatr Im S S Korsakova; 1989; 89(3):113-20. PubMed ID: 2728733 [TBL] [Abstract][Full Text] [Related]
33. Early myocardial disease and cramping myalgia in Becker-type muscular dystrophy: a kindred. Kuhn E; Fiehn W; Schröder JM; Assmus H; Wagner A Neurology; 1979 Aug; 29(8):1144-9. PubMed ID: 572500 [TBL] [Abstract][Full Text] [Related]
34. Mild and severe muscular dystrophy associated with deletions in Xp21 of the human X chromosome. Davies KE; Smith TJ; Bundey S; Read AP; Flint T; Bell M; Speer A J Med Genet; 1988 Jan; 25(1):9-13. PubMed ID: 3162536 [TBL] [Abstract][Full Text] [Related]
35. Reproductive fitness and frequency of new mutations in Becker muscular dystrophy: implications for genetic risk estimates. Passos-Bueno MR; Zatz M J Med Genet; 1991 Apr; 28(4):286-7. PubMed ID: 1856839 [No Abstract] [Full Text] [Related]
36. [Cardiomyopathy in female carriers of the Duchenne gene]. Wiegand V; Rahlf G; Meinck M; Kreuzer H Z Kardiol; 1984 Mar; 73(3):188-91. PubMed ID: 6719997 [TBL] [Abstract][Full Text] [Related]
37. New type of X-linked progressive muscular dystrophy involving shoulder girdle and back. Ji XW; Tan J; Chen XY; Yi SX; Liang H Am J Med Genet; 1990 Oct; 37(2):209-12. PubMed ID: 2248287 [TBL] [Abstract][Full Text] [Related]
38. The muscular dystrophies. Seiler J; Bope ET Am Fam Physician; 1986 Jul; 34(1):123-8. PubMed ID: 3728255 [TBL] [Abstract][Full Text] [Related]
39. [Importance of germ cell mosaic for genetic counseling of families with Duchenne and Becker muscular dystrophy]. Janka M; Grimm T Klin Padiatr; 1991; 203(5):354-8. PubMed ID: 1942941 [TBL] [Abstract][Full Text] [Related]
40. Chromosome 12-linked autosomal dominant scapuloperoneal muscular dystrophy. Wilhelmsen KC; Blake DM; Lynch T; Mabutas J; De Vera M; Neystat M; Bernstein M; Hirano M; Gilliam TC; Murphy PL; Sola MD; Bonilla E; Schotland DL; Hays AP; Rowland LP Ann Neurol; 1996 Apr; 39(4):507-20. PubMed ID: 8619529 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]