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3. [Echoscopic diagnosis of the heterozygote carrier state in Duchenne's muscular dystrophy]. Krasil'nikov VV; Lazebnik TA; Prokof'ev GV Zh Nevropatol Psikhiatr Im S S Korsakova; 1988; 88(11):18-9. PubMed ID: 3066080 [TBL] [Abstract][Full Text] [Related]
4. [New aspects of carrier diagnosis and human genetic counseling in Duchenne and Becker muscular dystrophy]. Spiegler AW; Huppert P; Werner W; Metzke H; Strobel U; Köhler K; Gerhardt R; Kaufmann J; Herrmann FH Z Arztl Fortbild (Jena); 1988; 82(22):1139-42. PubMed ID: 3247797 [No Abstract] [Full Text] [Related]
5. [Female transmitters of Duchenne's myopathy: detection by quantitative ultrasonography combined with blood creatine kinase]. Schapira G; Laugier P; Rochette J; Berger G; Katz P; Perrin J C R Acad Sci III; 1986; 303(10):377-80. PubMed ID: 3096500 [TBL] [Abstract][Full Text] [Related]
6. Duchenne's muscular dystrophy in six siblings. The case for early diagnosis and neonatal screening. Moosa A S Afr Med J; 1982 Nov; 62(21):765-7. PubMed ID: 7135141 [TBL] [Abstract][Full Text] [Related]
8. [Diagnosis of Duchenne's muscular dystrophy using recombinant DNA technics]. Lindlöf M; Ammälä P; Somer H; Somer M; Simola KO; de la Chapelle A Duodecim; 1985; 101(22):2184-91. PubMed ID: 3000726 [No Abstract] [Full Text] [Related]
9. [Importance of recombinant DNA studies for the identification of carriers of Duchenne's muscular dystrophy]. Veenema H; Leschot NJ; van Ommen GJ; Pearson PL Ned Tijdschr Geneeskd; 1985 Jun; 129(24):1137-41. PubMed ID: 4022155 [No Abstract] [Full Text] [Related]
10. [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]
11. [Duchenne's muscular dystrophy: also in girls?]. Ludescher E; Müller G; Ketelsen UP; Zellweger H; Ionasescu V Padiatr Padol; 1984; 19(2):161-6. PubMed ID: 6718041 [TBL] [Abstract][Full Text] [Related]
13. Dystrophin and Duchenne's muscular dystrophy. Hurko O; Johns DR N Engl J Med; 1989 Aug; 321(6):398-9. PubMed ID: 2664525 [No Abstract] [Full Text] [Related]
14. [Detection of the cause of genetic fault in Duchenne's dystrophy]. Palotie L; Somer H Duodecim; 1988; 104(20):1588-96. PubMed ID: 3056698 [No Abstract] [Full Text] [Related]
15. Sporadic Duchenne muscular dystrophy in females; genetic counseling of women with pelvifemoral muscular dystrophy. Zellweger H; Ionasescu V; Simpson J Helv Paediatr Acta; 1980 Sep; 35(4):343-8. PubMed ID: 7451237 [TBL] [Abstract][Full Text] [Related]
17. [Prevention of duchenne's muscular dystrophy: methodological problems in the detection of carriers (author's transl)]. Scarlato G; Valli G; Meola G Riv Patol Nerv Ment; 1977; 98(3):133-50. PubMed ID: 616016 [TBL] [Abstract][Full Text] [Related]
18. [Discriminant analysis of methods for detecting the heterozygote carrier state for the Duchenne muscular dystrophy gene]. Khrennikov VIu; Sitnikov VF; Deev AI; Svintsitskiĭ IV Zh Nevropatol Psikhiatr Im S S Korsakova; 1988; 88(11):14-8. PubMed ID: 3223151 [TBL] [Abstract][Full Text] [Related]
20. [Phenotype manifestation of disease in a heterozygote for Duchenne's form of muscular dystrophy]. Gencík A; Traubner P Cesk Neurol Neurochir; 1979 May; 42(3):205-11. PubMed ID: 455525 [No Abstract] [Full Text] [Related] [Next] [New Search]