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Journal Abstract Search

256 related items for PubMed ID: 8434633

  • 1. Decrease in the size of the myotonic dystrophy CTG repeat during transmission from parent to child: implications for genetic counselling and genetic anticipation.
    Hunter AG, Jacob P, O'Hoy K, MacDonald I, Mettler G, Tsilfidis C, Korneluk RG.
    Am J Med Genet; 1993 Feb 01; 45(3):401-7. PubMed ID: 8434633
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  • 2. Correlation between CTG trinucleotide repeat length and frequency of severe congenital myotonic dystrophy.
    Tsilfidis C, MacKenzie AE, Mettler G, Barceló J, Korneluk RG.
    Nat Genet; 1992 Jun 01; 1(3):192-5. PubMed ID: 1303233
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  • 3. [Correlation between degrees of the CTG repeat expansion and clinical features of myotonic dystrophy].
    Eguchi I, Koike R, Onodera O, Tanaka K, Kondo H, Tsuji S.
    Rinsho Shinkeigaku; 1994 Feb 01; 34(2):118-23. PubMed ID: 8194263
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  • 4. [DNA analysis of a pedigree with myotonic dystrophy in Songjiang county, Shanghai].
    Xie H, Zheng H, Zheng S, Deng B, Xu J, Cui Y, Wang Y, Xu Z, Ren D.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2000 Oct 01; 17(5):319-22. PubMed ID: 11024209
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  • 5. Myotonic dystrophy gene analysis in affected Israeli families.
    Achiron A, Magal N, Shem-Tov N, Noy S, Shohat M, Gadoth N.
    Isr J Med Sci; 1994 Aug 01; 30(8):622-5. PubMed ID: 8045745
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  • 6. An intergenerational contraction of the CTG repeat in Japanese myotonic dystrophy.
    Matsumura R, Namikawa T, Miki T, Kihira T, Yamagata H, Mano Y, Takayanagi T.
    J Neurol Sci; 1996 Jul 01; 139(1):48-51. PubMed ID: 8836971
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  • 7. Detection of the CTG repeat expansion in congenital myotonic dystrophy.
    Ohya K, Tachi N, Sato T, Kon S, Kikuchi K, Chiba S.
    Jpn J Hum Genet; 1997 Mar 01; 42(1):169-80. PubMed ID: 9183996
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  • 10. CTG instability in myotonic dystrophy: molecular genetic analysis of families from south-eastern France with characteristics of intergenerational variation in CGT repeat numbers.
    Duthel S, Bost M, Ollagnon E, Vial C, Petiot P, Chazot G, Vandenberghe A.
    Ann Genet; 1999 Mar 01; 42(3):151-9. PubMed ID: 10526658
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  • 11. The correlation of age of onset with CTG trinucleotide repeat amplification in myotonic dystrophy.
    Hunter A, Tsilfidis C, Mettler G, Jacob P, Mahadevan M, Surh L, Korneluk R.
    J Med Genet; 1992 Nov 01; 29(11):774-9. PubMed ID: 1453425
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  • 12. [Direct genotypic analysis of myotonic dystrophy: detection of an unstable DNA fragment in carriers].
    Cobo AM, Martorell L, López de Munain A, Basauri B, Martínez JM, Johnson K, Baiget M.
    Med Clin (Barc); 1993 Mar 13; 100(10):361-4. PubMed ID: 8097270
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  • 13. Prenatal diagnosis of congenital myotonic dystrophy and counseling of the pregnant mother: case report and literature review.
    Geifman-Holtzman O, Fay K.
    Am J Med Genet; 1998 Jul 07; 78(3):250-3. PubMed ID: 9677060
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  • 14. Myotonic dystrophy with no trinucleotide repeat expansion.
    Thornton CA, Griggs RC, Moxley RT.
    Ann Neurol; 1994 Mar 07; 35(3):269-72. PubMed ID: 8122879
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  • 15. Characteristics of dynamic mutation in Japanese myotonic dystrophy.
    Yamagata H, Miki T, Yamanaka N, Takemoto Y, Kanda F, Takahashi K, Inui T, Kinoshita M, Nakagawa M, Higuchi I.
    Jpn J Hum Genet; 1994 Sep 07; 39(3):327-35. PubMed ID: 7841443
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