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Journal Abstract Search

158 related items for PubMed ID: 2890571

  • 1. Familial deletion in Becker type muscular dystrophy within the pXJ region.
    Liechti-Gallati S, Braga S, Hirsiger H, Moser H.
    Hum Genet; 1987 Nov; 77(3):267-8. PubMed ID: 2890571
    [Abstract] [Full Text] [Related]

  • 2. DNA studies in a family with Duchenne muscular dystrophy and a deletion at Xp21.
    Greenberg CR, Hamerton JL, Nigli M, Wrogemann K.
    Am J Hum Genet; 1987 Aug; 41(2):128-37. PubMed ID: 3475976
    [Abstract] [Full Text] [Related]

  • 3. Molecular analysis of 25 Chinese families with Duchenne/Becker muscular dystrophy.
    Ko TM, Chen CF, Chiu HC, Hsieh FJ, Lee TY.
    J Formos Med Assoc; 1990 Oct; 89(10):850-6. PubMed ID: 1981771
    [Abstract] [Full Text] [Related]

  • 4. Localization and cloning of Xp21 deletion breakpoints involved in muscular dystrophy.
    Monaco AP, Bertelson CJ, Colletti-Feener C, Kunkel LM.
    Hum Genet; 1987 Mar; 75(3):221-7. PubMed ID: 2881877
    [Abstract] [Full Text] [Related]

  • 5. 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
    [Abstract] [Full Text] [Related]

  • 6. DNA analysis of Duchenne and Becker muscular dystrophy using pERT87 genomic probes and dystrophin cDNA probes--establishing the optimum strategy for carrier diagnosis in the Japanese population.
    Ubagai T, Katayama S.
    Jinrui Idengaku Zasshi; 1991 Sep; 36(3):211-27. PubMed ID: 1684391
    [Abstract] [Full Text] [Related]

  • 7. Molecular deletion analysis in Duchenne muscular dystrophy.
    Thomas NS, Ray PN, Worton RG, Harper PS.
    J Med Genet; 1986 Dec; 23(6):509-15. PubMed ID: 2879923
    [Abstract] [Full Text] [Related]

  • 8. Linkage studies in Duchenne and Becker muscular dystrophies.
    Walker A, Hart K, Cole C, Hodgson S, Johnson L, Dubowitz V, Bobrow M.
    J Med Genet; 1986 Dec; 23(6):538-47. PubMed ID: 2879925
    [Abstract] [Full Text] [Related]

  • 9. [Carrier detection and gene analysis in a Duchenne muscular dystrophy family].
    Lu FM.
    Zhonghua Shen Jing Jing Shen Ke Za Zhi; 1990 Aug; 23(4):231-3, 255. PubMed ID: 1979269
    [Abstract] [Full Text] [Related]

  • 10. 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
    [Abstract] [Full Text] [Related]

  • 11. Molecular analysis of human muscular dystrophies.
    Davies KE, Forrest S, Smith T, Kenwrick S, Ball S, Dorkins H, Patterson M.
    Muscle Nerve; 1987 Dec; 10(3):191-9. PubMed ID: 2882417
    [Abstract] [Full Text] [Related]

  • 12. DNA polymorphisms and deletion analysis of the Duchenne-Becker muscular dystrophy gene in the Chinese.
    Soong BW, Tsai TF, Su CH, Kao KP, Hsiao KJ, Su TS.
    Am J Med Genet; 1991 Mar 15; 38(4):593-600. PubMed ID: 1676564
    [Abstract] [Full Text] [Related]

  • 13. Segregation analysis of a marker localised Xp21.2-Xp21.3 in Duchenne and Becker muscular dystrophy families.
    Dorkins H, Junien C, Mandel JL, Wrogemann K, Moison JP, Martinez M, Old JM, Bundey S, Schwartz M, Carpenter N.
    Hum Genet; 1985 Mar 15; 71(2):103-7. PubMed ID: 2995231
    [Abstract] [Full Text] [Related]

  • 14. De novo DNA microdeletion in a girl with Turner syndrome and Duchenne muscular dystrophy.
    Chelly J, Marlhens F, Le Marec B, Jeanpierre M, Lambert M, Hamard G, Dutrillaux B, Kaplan JC.
    Hum Genet; 1986 Oct 15; 74(2):193-6. PubMed ID: 2876949
    [Abstract] [Full Text] [Related]

  • 15. Isolation of a random cosmid clone, cX5, which defines a new polymorphic locus DXS148 near the locus for Duchenne muscular dystrophy.
    Hofker MH, Bergen AA, Skraastad MI, Bakker E, Francke U, Wieringa B, Bartley J, van Ommen GJ, Pearson PL.
    Hum Genet; 1986 Nov 15; 74(3):275-9. PubMed ID: 2877936
    [Abstract] [Full Text] [Related]

  • 16. 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 15; 34(4):555-61. PubMed ID: 2576185
    [Abstract] [Full Text] [Related]

  • 17. Carrier detection and prenatal diagnosis in X linked muscular dystrophy using restriction fragment length polymorphisms.
    Lindlöf M, Kääriäinen H, Davies KE, de la Chapelle A.
    J Med Genet; 1986 Dec 15; 23(6):560-72. PubMed ID: 2879928
    [Abstract] [Full Text] [Related]

  • 18. Genetic counselling in Duchenne and Becker muscular dystrophy is problematic when carrier studies give controversial results.
    Kääriäinen H, Lindlöf M, Somer H, de la Chapelle A.
    Clin Genet; 1990 Mar 15; 37(3):179-87. PubMed ID: 1969777
    [Abstract] [Full Text] [Related]

  • 19. Brother/sister pairs affected with early-onset, progressive muscular dystrophy: molecular studies reveal etiologic heterogeneity.
    Francke U, Darras BT, Hersh JH, Berg BO, Miller RG.
    Am J Hum Genet; 1989 Jul 15; 45(1):63-72. PubMed ID: 2568091
    [Abstract] [Full Text] [Related]

  • 20. Deletion analysis of Duchenne muscular dystrophy using cDNA probes and multiplex PCR.
    Radosavljević D, Todorović D, Crkvenjakov R.
    Neurol Croat; 1991 Jul 15; 40(3):157-64. PubMed ID: 1681950
    [Abstract] [Full Text] [Related]

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