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Adenosine deaminase diagnosis

NEW PERSPECTIVES IN THE DIAGNOSIS AND TREATMENT OP ADENOSINE DEAMINASE (ADA) DEFICIENCY... [Pg.35]

J. Mejer and P. Nygaard, Adenosine deaminase and purine nucleoside phosphorylase levels in acute myeloblastic leukemia cells. Relationship to diagnosis and clinical course Leukemia Res.. 3 211 (1979). [Pg.252]

Figure 6.8 A family tree in which the proposita died of severe combined immunodeficiency. The arrow points to the infant in whom a prenatal diagnosis of adenosine deaminase deficiency was made. Under each symbol the ADA level is given by two different methods. The ADA genotype is given in brackets. Figure 6.8 A family tree in which the proposita died of severe combined immunodeficiency. The arrow points to the infant in whom a prenatal diagnosis of adenosine deaminase deficiency was made. Under each symbol the ADA level is given by two different methods. The ADA genotype is given in brackets.
See other pages where Adenosine deaminase diagnosis is mentioned: [Pg.246]    [Pg.518]    [Pg.506]    [Pg.54]    [Pg.113]    [Pg.449]   
See also in sourсe #XX -- [ Pg.33 , Pg.34 , Pg.35 , Pg.36 , Pg.37 ]



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