BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

178 related articles for article (PubMed ID: 1935912)

  • 1. Molecular analysis of X-autosome translocations in females with Duchenne muscular dystrophy.
    Bodrug SE; Holden JJ; Ray PN; Worton RG
    EMBO J; 1991 Dec; 10(12):3931-9. PubMed ID: 1935912
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Common sequence motifs at the rearrangement sites of a constitutional X/autosome translocation and associated deletion.
    Giacalone JP; Francke U
    Am J Hum Genet; 1992 Apr; 50(4):725-41. PubMed ID: 1347968
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mapping of four translocation breakpoints within the Duchenne muscular dystrophy gene.
    Bodrug SE; Burghes AH; Ray PM; Worton RG
    Genomics; 1989 Jan; 4(1):101-4. PubMed ID: 2914705
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Sequence analysis of the breakpoint regions of an X;5 translocation in a female with Duchenne muscular dystrophy.
    van Bakel I; Holt S; Craig I; Boyd Y
    Am J Hum Genet; 1995 Aug; 57(2):329-36. PubMed ID: 7668258
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mapping of X chromosome translocation breakpoints in females with Duchenne muscular dystrophy with respect to exons of the dystrophin gene.
    Cockburn DJ; Munro EA; Craig IW; Boyd Y
    Hum Genet; 1992 Dec; 90(4):407-12. PubMed ID: 1483697
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The parental origin of de novo X-autosome translocations in females with Duchenne muscular dystrophy revealed by M27 beta methylation analysis.
    Robinson DO; Boyd Y; Cockburn D; Collinson MN; Craig I; Jacobs PA
    Genet Res; 1990; 56(2-3):135-40. PubMed ID: 2272503
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Molecular analysis of a constitutional X-autosome translocation in a female with muscular dystrophy.
    Bodrug SE; Ray PN; Gonzalez IL; Schmickel RD; Sylvester JE; Worton RG
    Science; 1987 Sep; 237(4822):1620-4. PubMed ID: 3629260
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mapping of 12 translocation breakpoints in the Xp21 region with respect to the locus for Duchenne muscular dystrophy.
    Boyd Y; Cockburn D; Holt S; Munro E; Van Ommen GJ; Gillard B; Affara N; Ferguson-Smith M; Craig I
    Cytogenet Cell Genet; 1988; 48(1):28-34. PubMed ID: 3180845
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Prenatal identification of a girl with a t(X;4)(p21;q35) translocation: molecular characterisation, paternal origin, and association with muscular dystrophy.
    Bodrug SE; Roberson JR; Weiss L; Ray PN; Worton RG; Van Dyke DL
    J Med Genet; 1990 Jul; 27(7):426-32. PubMed ID: 2395160
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Muscular dystrophy in girls with X;autosome translocations.
    Boyd Y; Buckle V; Holt S; Munro E; Hunter D; Craig I
    J Med Genet; 1986 Dec; 23(6):484-90. PubMed ID: 3806636
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Duchenne muscular dystrophy: gene and gene product; mechanism of mutation in the gene.
    Worton RG
    J Inherit Metab Dis; 1992; 15(4):539-50. PubMed ID: 1528015
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Intragenic deletions in 21 Duchenne muscular dystrophy (DMD)/Becker muscular dystrophy (BMD) families studied with the dystrophin cDNA: location of breakpoints on HindIII and BglII exon-containing fragment maps, meiotic and mitotic origin of the mutations.
    Darras BT; Blattner P; Harper JF; Spiro AJ; Alter S; Francke U
    Am J Hum Genet; 1988 Nov; 43(5):620-9. PubMed ID: 2903663
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Sequences of junction fragments in the deletion-prone region of the dystrophin gene.
    Love DR; England SB; Speer A; Marsden RF; Bloomfield JF; Roche AL; Cross GS; Mountford RC; Smith TJ; Davies KE
    Genomics; 1991 May; 10(1):57-67. PubMed ID: 2045110
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Is gene deletion in eukaryotes sequence-dependent? A study of nine deletion junctions and nineteen other deletion breakpoints in intron 7 of the human dystrophin gene.
    McNaughton JC; Cockburn DJ; Hughes G; Jones WA; Laing NG; Ray PN; Stockwell PA; Petersen GB
    Gene; 1998 Nov; 222(1):41-51. PubMed ID: 9813236
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Molecular heterogeneity of translocations associated with muscular dystrophy.
    Boyd Y; Munro E; Ray P; Worton R; Monaco T; Kunkel L; Craig I
    Clin Genet; 1987 Apr; 31(4):265-72. PubMed ID: 3594934
    [TBL] [Abstract][Full Text] [Related]  

  • 16. X;autosome translocations in females with Duchenne or Becker muscular dystrophy.
    Dubowitz V
    Nature; 1986 Jul 17-23; 322(6076):291-2. PubMed ID: 3461282
    [No Abstract]   [Full Text] [Related]  

  • 17. 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]  

  • 18. Clinical features in a girl with Duchenne muscular dystrophy with an X-autosome translocation; (X;4)(p21;q26).
    Kimura S; Mitsuda T; Misugi N; Saito F; Tonomura A; Sugita H
    Brain Dev; 1986; 8(6):619-23. PubMed ID: 3826553
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Molecular genetic analysis of 67 patients with Duchenne/Becker muscular dystrophy.
    Niemann-Seyde S; Slomski R; Rininsland F; Ellermeyer U; Kwiatkowska J; Reiss J
    Hum Genet; 1992; 90(1-2):65-70. PubMed ID: 1427789
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The problem of Duchenne muscular dystrophy.
    Worton RG; Ray PN; Bodrug S; Burghes AH; Hu X; Thompson MW
    Philos Trans R Soc Lond B Biol Sci; 1988 Jun; 319(1194):275-84. PubMed ID: 2900521
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.