BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

173 related articles for article (PubMed ID: 9391889)

  • 1. Paternal transmission of congenital myotonic dystrophy.
    de Die-Smulders CE; Smeets HJ; Loots W; Anten HB; Mirandolle JF; Geraedts JP; Höweler CJ
    J Med Genet; 1997 Nov; 34(11):930-3. PubMed ID: 9391889
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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; 42(1):169-80. PubMed ID: 9183996
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Congenital myotonic dystrophy transmitted from an asymptomatic father with a DM-specific gene.
    Ohya K; Tachi N; Chiba S; Sato T; Kon S; Kikuchi K; Imamura S; Yamagata H; Miki T
    Neurology; 1994 Oct; 44(10):1958-60. PubMed ID: 7936256
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Paternal transmission of the congenital form of myotonic dystrophy type 1: a new case and review of the literature.
    Zeesman S; Carson N; Whelan DT
    Am J Med Genet; 2002 Jan; 107(3):222-6. PubMed ID: 11807903
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Haplotype analysis of congenital myotonic dystrophy patients from asymptomatic DM father.
    Tachi N; Ohya K; Yamagata H; Miki T; Kikuchi K; Chiba S
    Pediatr Neurol; 1997 May; 16(4):315-8. PubMed ID: 9258965
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 139(1):48-51. PubMed ID: 8836971
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Clinical and molecular genetic analyses of congenital myotonic dystrophy].
    Kojo T; Arahata K
    Nihon Rinsho; 1997 Dec; 55(12):3234-8. PubMed ID: 9436443
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A case of paternally inherited congenital myotonic dystrophy.
    Nakagawa M; Yamada H; Higuchi I; Kaminishi Y; Miki T; Johnson K; Osame M
    J Med Genet; 1994 May; 31(5):397-400. PubMed ID: 8064819
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Frequency of intergenerational contractions of the CTG repeats in myotonic dystrophy.
    López de Munain A; Cobo AM; Sáenz A; Blanco A; Poza JJ; Martorell L; Martí-Massó JF; Baiget M
    Genet Epidemiol; 1996; 13(5):483-7. PubMed ID: 8905394
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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; 1(3):192-5. PubMed ID: 1303233
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Paternal transmission of congenital myotonic dystrophy.
    Bergoffen J; Kant J; Sladky J; McDonald-McGinn D; Zackai EH; Fischbeck KH
    J Med Genet; 1994 Jul; 31(7):518-20. PubMed ID: 7966187
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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; 42(3):151-9. PubMed ID: 10526658
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [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; 17(5):319-22. PubMed ID: 11024209
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Congenital myotonic dystrophy: report of paternal transmission.
    Tanaka Y; Suzuki Y; Shimozawa N; Nanba E; Kondo N
    Brain Dev; 2000 Mar; 22(2):132-4. PubMed ID: 10722967
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Effects of the sex of myotonic dystrophy patients on the unstable triplet repeat in their affected offspring.
    Ashizawa T; Dunne PW; Ward PA; Seltzer WK; Richards CS
    Neurology; 1994 Jan; 44(1):120-2. PubMed ID: 8290046
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [DNA diagnosis in myotonic dystrophy].
    Tachi N
    Hokkaido Igaku Zasshi; 1996 Jan; 71(1):3-8. PubMed ID: 8727368
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Characteristics of intergenerational contractions of the CTG repeat in myotonic dystrophy.
    Ashizawa T; Anvret M; Baiget M; Barceló JM; Brunner H; Cobo AM; Dallapiccola B; Fenwick RG; Grandell U; Harley H
    Am J Hum Genet; 1994 Mar; 54(3):414-23. PubMed ID: 8116611
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Myotonic dystrophy: muscle involvement in relation to disease type and size of expanded CTG-repeat sequence.
    Kroksmark AK; Ekström AB; Björck E; Tulinius M
    Dev Med Child Neurol; 2005 Jul; 47(7):478-85. PubMed ID: 15991869
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Somatic cell heterogeneity between DNA extracted from lymphocytes and skeletal muscle in congenital myotonic dystrophy.
    Ohya K; Tachi N; Kon S; Kikuchi K; Chiba S
    Jpn J Hum Genet; 1995 Dec; 40(4):319-26. PubMed ID: 8851765
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Influence of sex of the transmitting parent as well as of parental allele size on the CTG expansion in myotonic dystrophy (DM).
    Brunner HG; Brüggenwirth HT; Nillesen W; Jansen G; Hamel BC; Hoppe RL; de Die CE; Höweler CJ; van Oost BA; Wieringa B
    Am J Hum Genet; 1993 Nov; 53(5):1016-23. PubMed ID: 8213829
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.