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2. Increased chloride efflux in fibroblasts from X-linked muscular dystrophies and clones from Duchenne carriers. Rugolo M; Rocchi M; Lenaz G; Romeo G FEBS Lett; 1987 Feb; 212(2):313-6. PubMed ID: 3817163 [TBL] [Abstract][Full Text] [Related]
3. Manifesting carrier of Becker muscular dystrophy (BMD): clinical and recombinant DNA studies. Ionasescu VV; Searby CC; Ionasescu R Acta Neurol Scand; 1989 Jun; 79(6):500-3. PubMed ID: 2782030 [TBL] [Abstract][Full Text] [Related]
4. Variability in clinical, genetic and protein abnormalities in manifesting carriers of Duchenne and Becker muscular dystrophy. Bushby KM; Goodship JA; Nicholson LV; Johnson MA; Haggerty ID; Gardner-Medwin D Neuromuscul Disord; 1993 Jan; 3(1):57-64. PubMed ID: 8329890 [TBL] [Abstract][Full Text] [Related]
5. An isolated case of Duchenne muscular dystrophy (DMD) in a female with a deletion of DMD cDNA. Yoshioka M; Yamamoto Y; Furuyama J Clin Genet; 1990 Dec; 38(6):474-8. PubMed ID: 2289321 [TBL] [Abstract][Full Text] [Related]
6. Dystrophin immunocytochemistry in muscle culture: detection of a carrier of Duchenne muscular dystrophy. Miranda AF; Francke U; Bonilla E; Martucci G; Schmidt B; Salviati G; Rubin M Am J Med Genet; 1989 Feb; 32(2):268-73. PubMed ID: 2648829 [TBL] [Abstract][Full Text] [Related]
7. Discordance of muscular dystrophy in monozygotic female twins: evidence supporting asymmetric splitting of the inner cell mass in a manifesting carrier of Duchenne dystrophy. Lupski JR; Garcia CA; Zoghbi HY; Hoffman EP; Fenwick RG Am J Med Genet; 1991 Sep; 40(3):354-64. PubMed ID: 1683155 [TBL] [Abstract][Full Text] [Related]
8. Skewed X inactivation in a female MZ twin results in Duchenne muscular dystrophy. Richards CS; Watkins SC; Hoffman EP; Schneider NR; Milsark IW; Katz KS; Cook JD; Kunkel LM; Cortada JM Am J Hum Genet; 1990 Apr; 46(4):672-81. PubMed ID: 2180286 [TBL] [Abstract][Full Text] [Related]
9. The clinical consequences of X-chromosome inactivation: Duchenne muscular dystrophy in one of monozygotic twins. Pena SD; Karpati G; Carpenter S; Fraser FC J Neurol Sci; 1987 Jul; 79(3):337-44. PubMed ID: 3612177 [TBL] [Abstract][Full Text] [Related]
15. X-linked and FSH dystrophies in one family. Lecky BR; MacKenzie JM; Read AP; Wilcox DE Neuromuscul Disord; 1991; 1(4):275-8. PubMed ID: 1822806 [TBL] [Abstract][Full Text] [Related]
16. Computed tomographic findings in manifesting carriers of Duchenne muscular dystrophy. de Visser M; Verbeeten B Clin Genet; 1985 Mar; 27(3):269-75. PubMed ID: 3987077 [TBL] [Abstract][Full Text] [Related]
17. Mosaic pattern of dystrophin in DMD. Emery A Pediatr Neurol; 1990; 6(4):282. PubMed ID: 2271043 [No Abstract] [Full Text] [Related]
18. Molecular genetics and genetic counselling for Duchenne/Becker muscular dystrophy. Laing NG Mol Cell Biol Hum Dis Ser; 1993; 3():37-84. PubMed ID: 8111545 [No Abstract] [Full Text] [Related]
19. 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]
20. Detection of Duchenne muscular dystrophy carriers by dosage analysis using the DMD cDNA clone 8. Mao YP; Cremer M Hum Genet; 1989 Jan; 81(2):193-5. PubMed ID: 2912889 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]