BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

254 related articles for article (PubMed ID: 6317539)

  • 21. DNA probe analysis for carrier detection and prenatal diagnosis of Duchenne muscular dystrophy: a standard diagnostic procedure.
    Bakker E; Bonten EJ; De Lange LF; Veenema H; Majoor-Krakauer D; Hofker MH; Van Ommen GJ; Pearson PL
    J Med Genet; 1986 Dec; 23(6):573-80. PubMed ID: 2879929
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Carrier detection and prenatal diagnosis in X linked muscular dystrophy using restriction fragment length polymorphisms.
    Lindlöf M; Kääriäinen H; Davies KE; de la Chapelle A
    J Med Genet; 1986 Dec; 23(6):560-72. PubMed ID: 2879928
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Molecular analysis of 25 Chinese families with Duchenne/Becker muscular dystrophy.
    Ko TM; Chen CF; Chiu HC; Hsieh FJ; Lee TY
    J Formos Med Assoc; 1990 Oct; 89(10):850-6. PubMed ID: 1981771
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Hot spot of recombination within DXS164 in the Duchenne muscular dystrophy gene.
    Grimm T; Müller B; Dreier M; Kind E; Bettecken T; Meng G; Müller CR
    Am J Hum Genet; 1989 Sep; 45(3):368-72. PubMed ID: 2570527
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Mapping of X-linked Becker muscular dystrophy through crossovers identified by DNA polymorphisms and by haplotype characterization in somatic cell hybrids.
    Roncuzzi L; Fadda S; Mochi M; Prosperi L; Sangiorgi S; Santamaria R; Sbarra D; Besana D; Morandi L; Rocchi M
    Am J Hum Genet; 1985 Mar; 37(2):407-17. PubMed ID: 2984927
    [TBL] [Abstract][Full Text] [Related]  

  • 26. X-linked agammaglobulinemia and the red blood cell determinants Xg and 12E7 are not closely linked.
    Mensink EJ; Schot JD; Tippett P; Ott J; Schuurman RK
    Hum Genet; 1984; 68(4):303-9. PubMed ID: 6595200
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Molecular-genetic study of Duchenne and Becker muscular dystrophies: deletion analyses of 45 Japanese patients and segregation analyses in their families with RFLPs based on the data from normal Japanese females.
    Sugino S; Fujishita S; Kamimura N; Matsumoto T; Wapenaar MC; Deng HX; Shibuya N; Miike T; Niikawa N
    Am J Med Genet; 1989 Dec; 34(4):555-61. PubMed ID: 2576185
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Accurate assessment of intragenic recombination frequency within the Duchenne muscular dystrophy gene.
    Abbs S; Roberts RG; Mathew CG; Bentley DR; Bobrow M
    Genomics; 1990 Aug; 7(4):602-6. PubMed ID: 1974880
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Localisation of the gene for Emery-Dreifuss muscular dystrophy to the distal long arm of the X chromosome.
    Thomas NS; Williams H; Elsas LJ; Hopkins LC; Sarfarazi M; Harper PS
    J Med Genet; 1986 Dec; 23(6):596-8. PubMed ID: 3100805
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Linkage studies in a new X-linked myopathy, suggesting exclusion of DMD locus and tentative assignment to distal Xq.
    Saviranta P; Lindlöf M; Lehesjoki AE; Kalimo H; Lang H; Sonninen V; Savontaus ML; de la Chapelle A
    Am J Hum Genet; 1988 Jan; 42(1):84-8. PubMed ID: 2892402
    [TBL] [Abstract][Full Text] [Related]  

  • 31. A linkage study of Emery-Dreifuss muscular dystrophy.
    Hodgson S; Boswinkel E; Cole C; Walker A; Dubowitz V; Granata C; Merlini L; Bobrow M
    Hum Genet; 1986 Dec; 74(4):409-16. PubMed ID: 3466853
    [TBL] [Abstract][Full Text] [Related]  

  • 32. A physical map of 4 million bp around the Duchenne muscular dystrophy gene on the human X-chromosome.
    van Ommen GJ; Verkerk JM; Hofker MH; Monaco AP; Kunkel LM; Ray P; Worton R; Wieringa B; Bakker E; Pearson PL
    Cell; 1986 Nov; 47(4):499-504. PubMed ID: 2877741
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Linked polymorphic DNA markers in the prediction of X-linked muscular dystrophy.
    Lindlöf M; Sistonen P; de la Chapelle A
    Ann Hum Genet; 1987 Oct; 51(4):317-28. PubMed ID: 3482147
    [TBL] [Abstract][Full Text] [Related]  

  • 34. A genetic linkage map of five marker loci in and around the Duchenne muscular dystrophy locus.
    Chen JD; Hejtmancik JF; Romeo G; Lindlof M; Boehm C; Caskey CT; Kress W; Fischbeck KH; Dreier M; Serravalle S
    Genomics; 1989 Jan; 4(1):105-9. PubMed ID: 2563349
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Assignment of Emery-Dreifuss muscular dystrophy to the distal region of Xq28: the results of a collaborative study.
    Consalez GG; Thomas NS; Stayton CL; Knight SJ; Johnson M; Hopkins LC; Harper PS; Elsas LJ; Warren ST
    Am J Hum Genet; 1991 Mar; 48(3):468-80. PubMed ID: 1998333
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Absence of genetic heterogeneity in Duchenne muscular dystrophy shown by a linkage study using two cloned DNA sequences.
    O'Brien T; Harper PS; Davies KE; Murray JM; Sarfarazi M; Williamson R
    J Med Genet; 1983 Aug; 20(4):249-51. PubMed ID: 6684692
    [TBL] [Abstract][Full Text] [Related]  

  • 37. X-linked dilated cardiomyopathy. Molecular genetic evidence of linkage to the Duchenne muscular dystrophy (dystrophin) gene at the Xp21 locus.
    Towbin JA; Hejtmancik JF; Brink P; Gelb B; Zhu XM; Chamberlain JS; McCabe ER; Swift M
    Circulation; 1993 Jun; 87(6):1854-65. PubMed ID: 8504498
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Carrier diagnosis of Duchenne muscular dystrophy using restriction fragment length polymorphisms.
    Hejtmancik JF; Harris SG; Tsao CC; Ward PA; Caskey CT
    Neurology; 1986 Dec; 36(12):1553-62. PubMed ID: 2878392
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Use of serum creatine kinase, pyruvate kinase, and genetic linkage for carrier detection in Duchenne and Becker dystrophy.
    Hyser CL; Griggs RC; Mendell JR; Polakowska R; Quirk S; Brooke MH; Fenichel GM; Doherty RA
    Neurology; 1987 Jan; 37(1):4-10. PubMed ID: 2879259
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Cloning of the breakpoint of an X;21 translocation associated with Duchenne muscular dystrophy.
    Ray PN; Belfall B; Duff C; Logan C; Kean V; Thompson MW; Sylvester JE; Gorski JL; Schmickel RD; Worton RG
    Nature; 1985 Dec 19-1986 Jan 1; 318(6047):672-5. PubMed ID: 3001530
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 13.