These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

135 related articles for article (PubMed ID: 2688826)

  • 1. Myotonic dystrophy: developments in molecular genetics.
    Shaw DJ; Harper PS
    Br Med Bull; 1989 Jul; 45(3):745-59. PubMed ID: 2688826
    [TBL] [Abstract][Full Text] [Related]  

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

  • 3. Definition of subchromosomal intervals around the myotonic dystrophy gene region at 19q.
    Schonk D; Coerwinkel-Driessen M; van Dalen I; Oerlemans F; Smeets B; Schepens J; Hulsebos T; Cockburn D; Boyd Y; Davis M
    Genomics; 1989 Apr; 4(3):384-96. PubMed ID: 2714797
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The apolipoprotein CII gene: subchromosomal localisation and linkage to the myotonic dystrophy locus.
    Shaw DJ; Meredith AL; Sarfarazi M; Huson SM; Brook JD; Myklebost O; Harper PS
    Hum Genet; 1985; 70(3):271-3. PubMed ID: 2991117
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Multiple pilomatrixomata and myotonic dystrophy: a familial association.
    Geh JL; Moss AL
    Br J Plast Surg; 1999 Mar; 52(2):143-5. PubMed ID: 10434894
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Establishment of the mouse chromosome 7 region with homology to the myotonic dystrophy region of human chromosome 19q.
    Cavanna JS; Greenfield AJ; Johnson KJ; Marks AR; Nadal-Ginard B; Brown SD
    Genomics; 1990 May; 7(1):12-8. PubMed ID: 1970795
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Radiation-reduced hybrids for the myotonic dystrophy locus.
    Brook JD; Zemelman BV; Hadingham K; Siciliano MJ; Crow S; Harley HG; Rundle SA; Buxton J; Johnson K; Almond JW
    Genomics; 1992 Jun; 13(2):243-50. PubMed ID: 1612584
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Cataract and myotonic dystrophy: the role of molecular diagnosis.
    Reardon W; MacMillan JC; Myring J; Harley HG; Rundle SA; Beck L; Harper PS; Shaw DJ
    Br J Ophthalmol; 1993 Sep; 77(9):579-83. PubMed ID: 8218057
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genetic mapping of a second myotonic dystrophy locus.
    Ranum LP; Rasmussen PF; Benzow KA; Koob MD; Day JW
    Nat Genet; 1998 Jun; 19(2):196-8. PubMed ID: 9620781
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Myotonic dystrophy: opportunities for prenatal prediction.
    Schrott HG; Omenn GS
    Neurology; 1975 Aug; 25(8):789-91. PubMed ID: 1171415
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Regional localisations and linkage relationships of seven RFLPs and myotonic dystrophy on chromosome 19.
    Shaw DJ; Meredith AL; Sarfarazi M; Harley HG; Huson SM; Brook JD; Bufton L; Litt M; Mohandas T; Harper PS
    Hum Genet; 1986 Nov; 74(3):262-6. PubMed ID: 2877933
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Segregation of linked probes to myotonic dystrophy in a family demonstrating that 152 and APOC2 are on the same side of DM on 19q.
    Johnson K; Nimmo E; Jones P; Weiss M; Savontaus ML; Anvret M; Bartlett R; Roses A; Shaw D; Harper PS
    Hum Genet; 1988 Dec; 80(4):379-81. PubMed ID: 3198115
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Definition of subchromosomal intervals around the myotonic dystrophy locus at 19q.
    Brunner H; Coerwinkel-Driessen M; Smeets B; Schonk D; Schepens J; Oerlemans F; Hamel B; Ropers H; Wieringa B
    Prog Clin Biol Res; 1989; 306():107-14. PubMed ID: 2740406
    [No Abstract]   [Full Text] [Related]  

  • 14. Identification of new DNA markers close to the myotonic dystrophy locus.
    Brook JD; Harley HG; Walsh KV; Rundle SA; Siciliano MJ; Harper PS; Shaw DJ
    J Med Genet; 1991 Feb; 28(2):84-8. PubMed ID: 1672160
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Current problems in myotonic dystrophy].
    Weglewski A; Juryńczyk J
    Neurol Neurochir Pol; 1998; 32(4):903-11. PubMed ID: 9864718
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Cloning of the essential myotonic dystrophy region and mapping of the putative defect.
    Aslanidis C; Jansen G; Amemiya C; Shutler G; Mahadevan M; Tsilfidis C; Chen C; Alleman J; Wormskamp NG; Vooijs M
    Nature; 1992 Feb; 355(6360):548-51. PubMed ID: 1346925
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Myotonic dystrophy: molecular genetics and diagnosis.
    Gharehbaghi-Schnell E; Finsterer J; Korschineck I; Mamoli B; Binder BR
    Wien Klin Wochenschr; 1998 Jan; 110(1):7-14. PubMed ID: 9499472
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Myotonic dystrophies.
    Meola G
    Curr Opin Neurol; 2000 Oct; 13(5):519-25. PubMed ID: 11073357
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Myotonic dystrophy type 2 and related myotonic disorders.
    Meola G; Moxley RT
    J Neurol; 2004 Oct; 251(10):1173-82. PubMed ID: 15503094
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Prenatal diagnosis of myotonic muscular dystrophy with linked deoxyribonucleic acid probes.
    Milunsky A; Skare JC; Milunsky JM; Maher TA; Amos JA
    Am J Obstet Gynecol; 1991 Mar; 164(3):751-5. PubMed ID: 2003536
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.