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Journal of the American Academy of Dermatology|October 1, 1992
Wiskott-Aldrich syndrome: new molecular and biochemical insightsM Peacocke, K A SiminovitchProceedings of the National Academy of Sciences of the United States of America|May 1, 1987
Linkage of the Wiskott-Aldrich syndrome with polymorphic DNA sequences from the human X chromosomeM Peacocke, K A SiminovitchHuman Genetics|February 1, 1992
The Wiskott-Aldrich syndrome: refinement of the localization on Xp and identification of another closely linked marker locus, OATL1W L Greer, M Peacocke, K A SiminovitchJournal of Investigative Medicine : the Official Publication of the American Federation for Clinical Research|April 1, 1995
A diagnostic assay for the Wiskott-Aldrich syndrome and its variant formsK A Siminovitch, W L Greer, A Novogrodsky, et al.Immunodeficiency|January 1, 1993
Selective impairment of CD43-mediated T cell activation in the Wiskott-Aldrich syndromeK A Siminovitch, W L Greer, B Axelsson, et al.Human Genetics|October 1, 1993
Linkage of Wiskott-Aldrich syndrome with three marker loci, DXS426, SYP and TFE3, which map to the Xp11.3-p11.22 regionS M Cremin, W L Greer, R Bodok-Nutzati, et al.Genomics|January 1, 1989
X-chromosome inactivation in the Wiskott-Aldrich syndrome: a marker for detection of the carrier state and identification of cell lineages expressing the gene defectW L Greer, P C Kwong, M Peacocke, et al.Genomics|March 1, 1990
Linkage relationships of the Wiskott-Aldrich syndrome to 10 loci in the pericentromeric region of the human X chromosomeW L Greer, A K Somani, P C Kwong, et al.Human Molecular Genetics|July 1, 1995
Identification of WASP mutations in patients with Wiskott-Aldrich syndrome and isolated thrombocytopenia reveals allelic heterogeneity at the WAS locusR Kolluri, A Shehabeldin, M Peacocke, et al.Pageof 15