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Journal Abstract Search

128 related items for PubMed ID: 7534923

  • 1. Prenatal diagnosis of xeroderma pigmentosum and Cockayne syndrome.
    Cleaver JE, Volpe JP, Charles WC, Thomas GH.
    Prenat Diagn; 1994 Oct; 14(10):921-8. PubMed ID: 7534923
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  • 2. DNA repair and ultraviolet mutagenesis in cells from a new patient with xeroderma pigmentosum group G and cockayne syndrome resemble xeroderma pigmentosum cells.
    Moriwaki S, Stefanini M, Lehmann AR, Hoeijmakers JH, Robbins JH, Rapin I, Botta E, Tanganelli B, Vermeulen W, Broughton BC, Kraemer KH.
    J Invest Dermatol; 1996 Oct; 107(4):647-53. PubMed ID: 8823375
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  • 3. Cerebro-oculo-facio-skeletal syndrome with a nucleotide excision-repair defect and a mutated XPD gene, with prenatal diagnosis in a triplet pregnancy.
    Graham JM, Anyane-Yeboa K, Raams A, Appeldoorn E, Kleijer WJ, Garritsen VH, Busch D, Edersheim TG, Jaspers NG.
    Am J Hum Genet; 2001 Aug; 69(2):291-300. PubMed ID: 11443545
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  • 4. [The determination of the complementation groups for the cells of patients with xeroderma pigmentosum and the Cockayne syndrome found in Russia].
    Pleskach NM, Mikhel'son VM, Raams A, Bootsma D.
    Tsitologiia; 1996 Aug; 38(8):863-8. PubMed ID: 9027016
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  • 5. Cockayne syndrome complementation group B associated with xeroderma pigmentosum phenotype.
    Itoh T, Cleaver JE, Yamaizumi M.
    Hum Genet; 1996 Feb; 97(2):176-9. PubMed ID: 8566949
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  • 6. Cockayne syndrome and xeroderma pigmentosum.
    Rapin I, Lindenbaum Y, Dickson DW, Kraemer KH, Robbins JH.
    Neurology; 2000 Nov 28; 55(10):1442-9. PubMed ID: 11185579
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  • 7. Cells from XP-D and XP-D-CS patients exhibit equally inefficient repair of UV-induced damage in transcribed genes but different capacity to recover UV-inhibited transcription.
    van Hoffen A, Kalle WH, de Jong-Versteeg A, Lehmann AR, van Zeeland AA, Mullenders LH.
    Nucleic Acids Res; 1999 Jul 15; 27(14):2898-904. PubMed ID: 10390531
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  • 8. Complementation of transformed fibroblasts from patients with combined xeroderma pigmentosum-Cockayne syndrome.
    Ellison AR, Nouspikel T, Jaspers NG, Clarkson SG, Gruenert DC.
    Exp Cell Res; 1998 Aug 25; 243(1):22-8. PubMed ID: 9716445
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  • 10. Xeroderma pigmentosum complementation group G associated with Cockayne syndrome.
    Vermeulen W, Jaeken J, Jaspers NG, Bootsma D, Hoeijmakers JH.
    Am J Hum Genet; 1993 Jul 25; 53(1):185-92. PubMed ID: 8317483
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  • 18. Xeroderma pigmentosum and Cockayne syndrome: overlapping clinical and biochemical phenotypes.
    Greenhaw GA, Hebert A, Duke-Woodside ME, Butler IJ, Hecht JT, Cleaver JE, Thomas GH, Horton WA.
    Am J Hum Genet; 1992 Apr 25; 50(4):677-89. PubMed ID: 1372469
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  • 19. A new UV-sensitive syndrome not belonging to any complementation groups of xeroderma pigmentosum or Cockayne syndrome: siblings showing biochemical characteristics of Cockayne syndrome without typical clinical manifestations.
    Itoh T, Ono T, Yamaizumi M.
    Mutat Res; 1994 May 25; 314(3):233-48. PubMed ID: 7513056
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