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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

202 related items for PubMed ID: 1968008

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  • 5. Molecular-genetic study of Duchenne and Becker muscular dystrophies: deletion analyses of 45 Japanese patients and segregation analyses in their families with RFLPs based on the data from normal Japanese females.
    Sugino S, Fujishita S, Kamimura N, Matsumoto T, Wapenaar MC, Deng HX, Shibuya N, Miike T, Niikawa N.
    Am J Med Genet; 1989 Dec; 34(4):555-61. PubMed ID: 2576185
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  • 6. Prenatal diagnosis and carrier detection by DNA studies in a Duchenne muscular dystrophy family with no living affected male.
    Chen JD, Denton MJ, Serravalle S, Morgan G.
    Aust Paediatr J; 1988 Dec; 24(6):351-3. PubMed ID: 2907402
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  • 7. The diagnosis of Duchenne and Becker muscular dystrophies: two years' experience in a comprehensive carrier screening and prenatal diagnostic laboratory.
    Laing NG, Mears ME, Chandler DC, Layton MG, Thomas HE, Johnsen RD, Goldblatt J, Kakulas BA.
    Med J Aust; 1991 Jan 07; 154(1):14-8. PubMed ID: 1670611
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  • 8. Effective strategy for prenatal prediction of Duchenne and Becker muscular dystrophy.
    Forrest SM, Smith TJ, Cross GS, Read AP, Thomas NS, Mountford RC, Harper PS, Geirsson RT, Davies KE.
    Lancet; 1987 Dec 05; 2(8571):1294-7. PubMed ID: 2890901
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  • 11. Analysis of RFLPs and DNA deletions in the Chinese Duchenne muscular dystrophy gene.
    Zeng YT, Chen MJ, Ren ZR, Qui XK, Huang SZ.
    J Med Genet; 1991 Mar 05; 28(3):167-70. PubMed ID: 1675685
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  • 15. Carrier diagnosis of Duchenne muscular dystrophy using restriction fragment length polymorphisms.
    Hejtmancik JF, Harris SG, Tsao CC, Ward PA, Caskey CT.
    Neurology; 1986 Dec 05; 36(12):1553-62. PubMed ID: 2878392
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  • 19. Molecular biological approaches to genetic disorders in prenatal diagnosis.
    Katayama S.
    Early Hum Dev; 1992 Dec 05; 29(1-3):149-53. PubMed ID: 1356752
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