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Journal Abstract Search

104 related items for PubMed ID: 3398874

  • 1. Becker muscular dystrophy recombinant DNA studies in identical twins.
    Ionasescu V, Ionasescu R, Searby C, Burns T.
    Muscle Nerve; 1988 Apr; 11(4):287-90. PubMed ID: 3398874
    [Abstract] [Full Text] [Related]

  • 2. Duchenne muscular dystrophy in monozygotic twins: deletion of 5' fragments of the gene.
    Ionasescu VV, Searby CC, Ionasescu R, Patil S.
    Am J Med Genet; 1989 May; 33(1):113-6. PubMed ID: 2750778
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  • 3. 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 01; 40(3):354-64. PubMed ID: 1683155
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  • 4. [Spinal form of Ullrich's disease in monozygotic twins].
    Aver'ianov IuN, Il'ina NA, Mazaeva IV, Berezova NIu.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1982 Sep 01; 82(3):51-4. PubMed ID: 7200707
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  • 5. Emery-Dreifuss muscular dystrophy with unusual features.
    Deymeer F, Oge AE, Bayindir C, Kaymaz C, Nişanci Y, Adalet K, Yates JR, Ozdemir C.
    Muscle Nerve; 1993 Dec 01; 16(12):1359-65. PubMed ID: 8232393
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  • 6. Additional case of female monozygotic twins discordant for the clinical manifestations of Duchenne muscular dystrophy due to opposite X-chromosome inactivation.
    Abbadi N, Philippe C, Chery M, Gilgenkrantz H, Tome F, Collin H, Theau D, Recan D, Broux O, Fardeau M.
    Am J Med Genet; 1994 Aug 15; 52(2):198-206. PubMed ID: 7802009
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  • 9. Monozygotic female twin carriers discordant for the clinical manifestations of Duchenne muscular dystrophy.
    Chutkow JG, Hyser CL, Edwards JA, Heffner RR, Czyrny JJ.
    Neurology; 1987 Jul 15; 37(7):1147-51. PubMed ID: 2885783
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  • 11. Chromosome 4q DNA rearrangement in monozygotic twins discordant for facioscapulohumeral muscular dystrophy.
    Tawil R, Storvick D, Weiffenbach B, Altherr MR, Feasby TE, Griggs RC.
    Hum Mutat; 1993 Jul 15; 2(6):492-4. PubMed ID: 8111417
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  • 13. Treatment of Duchenne muscular dystrophy with growth hormone inhibitors.
    Zatz M, Betti RT, Frota-Pessoa O.
    Am J Med Genet; 1986 Jul 15; 24(3):549-66. PubMed ID: 3524231
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  • 15. [Association of sporadic limb-girdle muscular dystrophy and autonomous thyroid nodule in 3 Germans].
    Di Lorenzo L, Lupoli G, Cosentini E, Rippa PG, Lombardi G.
    Minerva Endocrinol; 1991 Jul 15; 16(3):147-51. PubMed ID: 1806812
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  • 16. [Monozygotic twins with progressive muscular dystrophy].
    Radu H, Killyen I, Rosu AM, Ionescu V.
    Z Neurol; 1972 Jul 15; 202(3):241-6. PubMed ID: 4120053
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  • 17. In situ hybridization shows direct evidence of skewed X inactivation in one of monozygotic twin females manifesting Duchenne muscular dystrophy.
    Zneimer SM, Schneider NR, Richards CS.
    Am J Med Genet; 1993 Mar 01; 45(5):601-5. PubMed ID: 8456832
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  • 18. [Muscular dystrophy of the Becker type].
    Carbajal-Rodríguez L, de Quevedo JJ, Loredo-Abdalá A, Villaseñor-Zepeda J.
    Bol Med Hosp Infant Mex; 1988 Sep 01; 45(9):605-9. PubMed ID: 3190853
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  • 20. Carrier detection in Duchenne and Becker muscular dystrophy using dinucleotide repeat polymorphisms. A study in Mexican families.
    Arenas D, Coral R, Cisneros B, Peñaloza L, Salamanca F, Kofman S, Mercado R, Méndez J, Martínez C, Montañez C.
    Arch Med Res; 1996 Sep 01; 27(2):151-6. PubMed ID: 8696057
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