Search Results - Flejter, W.L.

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  1. 1
    Correction of Xeroderma Pigmentosum Complementation Group D Mutant Cell Phenotypes by Chromosome and Gene Transfer: Involvement of the Human ERCC2 DNA Repair Gene

    Correction of Xeroderma Pigmentosum Complementation Group D Mutant Cell Phenotypes by Chromosome and Gene Transfer: Involvement of the Human ERCC2 DNA Repair Gene by Flejter, Wendy L., McDaniel, Lisa D., Johns, David, Friedberg, Errol C., Schultz, Roger A.

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  2. 2
    Region-specific cosmids and STRPs identified by chromosome microdissection and fish

    Region-specific cosmids and STRPs identified by chromosome microdissection and fish by Flejter, Wendy L., Bennett-Baker, Pamela, Barcroft, Christine L., Kiousis, Sam, Chamberlain, Jeffrey S.

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    Molecular cytogenetic analysis of Inv Dup(15) chromosomes, using probes specific for the Pradar-Willi/Angelman syndrome region: Clinical implications

    Molecular cytogenetic analysis of Inv Dup(15) chromosomes, using probes specific for the Pradar-Willi/Angelman syndrome region: Clinical implications by Leana-Cox, J., Jenkins, L., Palmer, C.G., Plattner, R., Sheppard, L., Flejter, W.L., Zackowski, J., Tsien, F., Schwartz, S.

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