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9. Becker-type muscular dystrophy. Report of a family with one postmortem study. Martin JJ; Leroy J; Ceuterick C; Lübke U; Van Buggenhout E; Van Vuchelen J; Van Broeckhoven C Clin Neurol Neurosurg; 1992; 94 Suppl():S123-6. PubMed ID: 1320486 [TBL] [Abstract][Full Text] [Related]
10. A grandpaternally derived de novo deletion within Xp21 initially presenting in carrier females diagnosed as Kugelberg-Welander syndrome. Wood S; Shukin RJ; McGillivray BC; Ray PN; Worton RG Am J Med Genet; 1988 Feb; 29(2):419-23. PubMed ID: 2895584 [TBL] [Abstract][Full Text] [Related]
11. Closing in on the muscular dystrophy gene. Kolata G Science; 1985 Oct; 230(4723):307-8. PubMed ID: 4048935 [No Abstract] [Full Text] [Related]
12. 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]
13. [X-chromosomal recessive spinobulbar muscular atrophy (Kennedy type). Description of a family, clinical aspects, molecular genetics, differential diagnosis and therapy]. Kuhlenbäumer G; Bocchicchio M; Kress W; Young P; Oberwittler C; Stögbauer F Nervenarzt; 1998 Aug; 69(8):660-5. PubMed ID: 9757416 [TBL] [Abstract][Full Text] [Related]
14. Deletion on the X chromosome detected by direct DNA analysis in one of two unrelated boys with glycerol kinase deficiency, adrenal hypoplasia, and Duchenne muscular dystrophy. Dunger DB; Davies KE; Pembrey M; Lake B; Pearson P; Williams D; Whitfield A; Dillon MJ Lancet; 1986 Mar; 1(8481):585-7. PubMed ID: 2869305 [TBL] [Abstract][Full Text] [Related]
15. [Differential diagnosis of a benign course of muscular dystrophy using molecular genetic methods]. Wagner M; Diedrich U; Pozsàr C; Becker PE; Reiss J Nervenarzt; 1990 Apr; 61(4):244-7. PubMed ID: 2352571 [No Abstract] [Full Text] [Related]
17. The Duchenne dystrophy story: from phenotype to gene and potential treatment. Dubowitz V J Child Neurol; 1989 Oct; 4(4):240-50. PubMed ID: 2677113 [No Abstract] [Full Text] [Related]
18. The new genetics and its application in the study of childhood muscular dystrophies. Chakravarty A; Chatterjee S J Assoc Physicians India; 1991 Dec; 39(12):943-8. PubMed ID: 1816224 [No Abstract] [Full Text] [Related]
19. 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]
20. Limb-girdle muscular dystrophy or spinal muscular atrophy: a source of diagnostic confusion? Pogue R; Jackson T; Sayli B; Curtis A; Bushby KM J Med Genet; 1997 Nov; 34(11):958-9. PubMed ID: 9391899 [No Abstract] [Full Text] [Related] [Next] [New Search]