BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

158 related articles for article (PubMed ID: 3712394)

  • 1. Duchenne muscular dystrophy in a female with a translocation involving Xp21.
    Nevin NC; Hughes AE; Calwell M; Lim JH
    J Med Genet; 1986 Apr; 23(2):171-3. PubMed ID: 3712394
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Expression of an X-linked muscular dystrophy in a female due to translocation involving Xp21 and non-random inactivation of the normal X chromosome.
    Verellen-Dumoulin C; Freund M; De Meyer R; Laterre C; Frédéric J; Thompson MW; Markovic VD; Worton RG
    Hum Genet; 1984; 67(1):115-9. PubMed ID: 6745920
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Duchenne muscular dystrophy (DMD) in a female with an X/autosome translocation: further evidence that the DMD locus is at Xp21.
    Jacobs PA; Hunt PA; Mayer M; Bart RD
    Am J Hum Genet; 1981 Jul; 33(4):513-8. PubMed ID: 7258185
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Translocation (X;6) in a female with Duchenne muscular dystrophy: implications for the localisation of the DMD locus.
    Zatz M; Vianna-Morgante AM; Campos P; Diament AJ
    J Med Genet; 1981 Dec; 18(6):442-7. PubMed ID: 7334502
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Duchenne muscular dystrophy in a girl with an (X;15) translocation.
    Ribeiro MC; Melaragno MI; Schmidt B; Brunoni D; Gabbai AA; Hackel C
    Am J Med Genet; 1986 Oct; 25(2):231-6. PubMed ID: 3777020
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Further evidence for Xp21 location of Duchenne muscular dystrophy (DMD) locus: X;9 translocation in a female with DMD.
    Emanuel BS; Zackai EH; Tucker SH
    J Med Genet; 1983 Dec; 20(6):461-3. PubMed ID: 6655672
    [TBL] [Abstract][Full Text] [Related]  

  • 8. High-resolution banding study of an X/4 translocation in a female with Duchenne muscular dystrophy.
    Saito F; Tonomura A; Kimura S; Misugi N; Sugita H
    Hum Genet; 1985; 71(4):370-1. PubMed ID: 4077054
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Xp21/autosome translocations. Case report and risk for Duchenne muscular dystrophy.
    Holden JJ; Smith A; MacLeod PM; Masotti R; Duncan AM
    Clin Genet; 1986 Jun; 29(6):516-22. PubMed ID: 3742857
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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]  

  • 13. 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]  

  • 14. Turner's syndrome and Duchenne muscular dystrophy in a girl with an X; autosome translocation.
    Bjerglund Nielsen L; Nielsen IM
    Ann Genet; 1984; 27(3):173-7. PubMed ID: 6334482
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. 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]  

  • 17. 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]  

  • 18. 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]  

  • 19. [Duchenne muscular dystrophy (DMD) in a female with an X-autosome translocation].
    Uchida T; Ogata H; Shirai Z; Mitsudome A
    No To Hattatsu; 1988 Jan; 20(1):28-32. PubMed ID: 3279979
    [No Abstract]   [Full Text] [Related]  

  • 20. Muscular dystrophy in an X; 1 translocation female suggests that Duchenne locus is on X chromosome short arm.
    Lindenbaum RH; Clarke G; Patel C; Moncrieff M; Hughes JT
    J Med Genet; 1979 Oct; 16(5):389-92. PubMed ID: 513085
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.