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Prenatal Diagnosis|March 12, 1999
Prenatal molecular diagnosis of Wiskott-Aldrich syndrome by direct mutation analysisS Giliani, M Fiorini, P Mella, et al.Immunological Reviews|February 24, 2001
Of genes and phenotypes: the immunological and molecular spectrum of combined immune deficiency. Defects of the gamma(c)-JAK3 signaling pathway as a modelL D Notarangelo, S Giliani, C Mazza, et al.Blood|November 14, 1997
Structural and functional basis for JAK3-deficient severe combined immunodeficiencyF Candotti, S A Oakes, J A Johnston, et al.Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|January 3, 2001
Neuroblastoma with symptomatic spinal cord compression at diagnosis: treatment and results with 76 casesDe Bernardi B, C Pianca, P Pistamiglio, et al.Genes and Immunity|January 10, 2002
Unexpected and variable phenotypes in a family with JAK3 deficiencyD M Frucht, M Gadina, G J Jagadeesh, et al.Advances in Genetics|October 19, 2000
Primary immunodeficiency mutation databasesM Vihinen, F X Arredondo-Vega, J L Casanova, et al.Pageof 3