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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

349 related items for PubMed ID: 7902070

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  • 2. Dystrophic forms of epidermolysis bullosa.
    Uitto J, Christiano AM.
    Semin Dermatol; 1993 Sep; 12(3):191-201. PubMed ID: 8217558
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  • 7. Prenatal diagnosis of Herlitz junctional epidermolysis bullosa in nonidentical twins.
    Fassihi H, Ashton GH, Denyer J, Mellerio JE, Mason G, McGrath JA.
    Clin Exp Dermatol; 2005 Mar; 30(2):180-2. PubMed ID: 15725250
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  • 9. Alport syndrome. Molecular genetic aspects.
    Hertz JM.
    Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
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  • 11. Single cell PCR amplification of microsatellites flanking the COL7A1 gene and suitability for preimplantation genetic diagnosis of Hallopeau-Siemens recessive dystrophic epidermolysis bullosa.
    Fassihi H, Renwick PJ, Black C, McGrath JA.
    J Dermatol Sci; 2006 Jun; 42(3):241-8. PubMed ID: 16500083
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  • 13. Prenatal diagnosis of severe dermatologic diseases.
    Sybert VP, Holbrook KA, Levy M.
    Adv Dermatol; 1992 Jun; 7():179-209; discussion 210. PubMed ID: 1739580
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  • 15. Carrier detection and prenatal diagnosis in haemophilia A and B.
    Chistolini A, Papacchini M, Mazzucconi MG, La Verde G, Arcieri R, Ferrari A, Paesano R, Pachi A, Mariani G.
    Haematologica; 1990 Jun; 75(5):424-8. PubMed ID: 1982946
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  • 20. Haemophilia management: the application of DNA analysis for prenatal diagnosis.
    Van de Water NS, Ockelford PA, Berry EW, Browett PJ.
    N Z Med J; 1991 Oct 23; 104(922):443-6. PubMed ID: 1681487
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