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9. Carrier detection in Duchenne muscular dystrophy by use of cloned DNA sequences. Wieacker P; Davies K; Pearson P; Ropers HH Lancet; 1983 Jun; 1(8337):1325-6. PubMed ID: 6134107 [No Abstract] [Full Text] [Related]
10. Studies of the carrier state in the Duchenne type of muscular dystrophy. 2. Quantitative electromyography as a method of carrier detection. Gardner-Medwin D J Neurol Neurosurg Psychiatry; 1968 Apr; 31(2):124-34. PubMed ID: 5684019 [No Abstract] [Full Text] [Related]
11. Lymphocyte capping and carrier detection in Duchenne muscular dystrophy. Br Med J; 1978 Dec; 2(6152):1589-90. PubMed ID: 728736 [No Abstract] [Full Text] [Related]
12. Detection of carriers of human Duchenne muscular dystrophy by freeze-fracture analysis of erythrocyte plasmalemmal intramembrane particles. Shivers RR; Martin K; Atkinson BG Am J Clin Pathol; 1986 Feb; 85(2):131-4. PubMed ID: 3946298 [TBL] [Abstract][Full Text] [Related]
13. Gallium-67 citrate localization in carriers of Duchenne muscular dystrophy. Brown RG; Ash JM; Verellen-Dumoulin C; Percy ME; Chang LS; Oss I; Fulford P Int J Nucl Med Biol; 1981; 8(4):379-88. PubMed ID: 6948790 [No Abstract] [Full Text] [Related]
14. Carrier detection in Duchenne muscular dystrophy: Assessment of the effect of age on detection-rate with serum-creatine-kinase-activity. Nicholson GA; Gardner-Medwin D; Pennington RJ; Walton JN Lancet; 1979 Mar; 1(8118):692-4. PubMed ID: 85935 [TBL] [Abstract][Full Text] [Related]