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 *

84 related articles for article (PubMed ID: 9608771)

  • 1. [Mutation analysis in the CTG-base multiplication in a family with myotonic dystrophy in three generations].
    Molnár J; Kis A; Melegh B; Nádasi E; Varjas T; Kovács E; Kosztolanyi G
    Orv Hetil; 1998 May; 139(18):1083-5. PubMed ID: 9608771
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Expansion and mutation rate in CTG repeats in the myotonic dystrophy gene].
    Khidiiatova IM; Fatkhlislamova RI; Magzhanov RV; Popova SN; Slominskiĭ PA; Limborskaia SA; Khusnutdinova EK
    Genetika; 2000 Oct; 36(10):1410-3. PubMed ID: 11094756
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Instability of a premutation allele in homozygous patients with myotonic dystrophy type 1.
    Abbruzzese C; Costanzi Porrini S; Mariani B; Gould FK; McAbney JP; Monckton DG; Ashizawa T; Giacanelli M
    Ann Neurol; 2002 Oct; 52(4):435-41. PubMed ID: 12325072
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Analysis of expansion of the triplet repeat (CTG)n in myotonic dystrophy patients from Bashkir].
    Slominskiĭ PA; Popova SN; Fatkhlislamova RI; Akhmadeeva LR; Magzhanov RV; Khusnutdinova EK; Limborskaia SA
    Genetika; 2000 Jun; 36(6):844-8. PubMed ID: 10923268
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [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]  

  • 6. Effect of triplet repeat expansion on chromatin structure and expression of DMPK and neighboring genes, SIX5 and DMWD, in myotonic dystrophy.
    Frisch R; Singleton KR; Moses PA; Gonzalez IL; Carango P; Marks HG; Funanage VL
    Mol Genet Metab; 2001; 74(1-2):281-91. PubMed ID: 11592825
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Characterization and polymerase chain reaction (PCR) detection of an Alu deletion polymorphism in total linkage disequilibrium with myotonic dystrophy.
    Mahadevan MS; Foitzik MA; Surh LC; Korneluk RG
    Genomics; 1993 Feb; 15(2):446-8. PubMed ID: 8449517
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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; 78(3):250-3. PubMed ID: 9677060
    [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. Characteristics of myotonic dystrophy in Istria: molecular genetics approach--mutation analysis.
    Medica I; Logar N; Batagelj M; Peterlin B
    Coll Antropol; 1998 Dec; 22(2):477-84. PubMed ID: 9887603
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. New methods for molecular diagnosis and demonstration of the (CCTG)n mutation in myotonic dystrophy type 2 (DM2).
    Sallinen R; Vihola A; Bachinski LL; Huoponen K; Haapasalo H; Hackman P; Zhang S; Sirito M; Kalimo H; Meola G; Horelli-Kuitunen N; Wessman M; Krahe R; Udd B
    Neuromuscul Disord; 2004 Apr; 14(4):274-83. PubMed ID: 15019706
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [From gene to disease; altered RNA processing as a cause of myotonic dystrophy type 1].
    de Die-Smulders CE; Faber CG; Smeets HJ
    Ned Tijdschr Geneeskd; 2005 Sep; 149(37):2043-6. PubMed ID: 16184945
    [TBL] [Abstract][Full Text] [Related]  

  • 14. DNA analysis in a suspected individual with myotonic dystrophy family history and her abortus.
    Bi X; Xie H; Zheng H; Ding S; Zhang S; Wang Y; Xu Z; Ren D
    Chin Med J (Engl); 2002 Nov; 115(11):1628-31. PubMed ID: 12609075
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Haplotype analysis of the DM1 locus in the Serbian population.
    Krndija D; Savić D; Mladenović J; Rakocević-Stojanović V; Apostolski S; Todorović S; Romac S
    Acta Neurol Scand; 2005 Apr; 111(4):274-7. PubMed ID: 15740580
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [A pedigree with myotonic dystrophy: non-CTG, non-CCTG repeat expansion].
    Zhao XP; Xie HJ; Zheng HM; Yu ZL; Cui Y; Ding SJ; Ren DM; Tang GM
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Oct; 21(5):459-62. PubMed ID: 15476170
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [DNA diagnosis of myotonic dystrophy in a family].
    Kihara K; Yamagata H; Miki T; Ogihara T
    Rinsho Shinkeigaku; 1993 Mar; 33(3):266-70. PubMed ID: 8334788
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A long PCR-based molecular protocol for detecting normal and expanded ZNF9 alleles in myotonic dystrophy type 2.
    Bonifazi E; Vallo L; Giardina E; Botta A; Novelli G
    Diagn Mol Pathol; 2004 Sep; 13(3):164-6. PubMed ID: 15322428
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 250 CTG repeats in DMPK is a threshold for correlation of expansion size and age at onset of juvenile-adult DM1.
    Savić D; Rakocvic-Stojanovic V; Keckarevic D; Culjkovic B; Stojkovic O; Mladenovic J; Todorovic S; Apostolski S; Romac S
    Hum Mutat; 2002 Feb; 19(2):131-9. PubMed ID: 11793472
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Somatic mosaicism of p(CTG)n expansion in a case of myotonic dystrophy with parotid tumor].
    Ogata K; Takahashi A; Oguchi N; Ishitoya J; Fuse S; Shimpo T
    Rinsho Shinkeigaku; 1998 Aug; 38(8):736-8. PubMed ID: 9916519
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.