deist

n.

自然神论信仰者；

Mutations in Fas associated with human lymphoproliferative syndrome and autoimmunity
Artemis, a Novel DNA Double-Strand Break Repair/V(D)J Recombination Protein, Is Mutated in Human Severe Combined Immune Deficiency
Perforin Gene Defects in Familial Hemophagocytic Lymphohistiocytosis
A serious adverse event after successful gene therapy for X- linked severe combined immunodeficiency [letter]
Erratum: Sustained correction of X-linked severe combined immunodeficiency by ex vivo gene therapy (New England Journal of Medicine ...
Low Penetrance, Broad Resistance, and Favorable Outcome of Interleukin 12 Receptor β1 Deficiency: Medical and Immunological Implica...
Survival advantage for irinotecan versus best supportive care as second-line chemotherapy in gastric cancer--a randomised phase III ...
Iatrogenic keratectasia after laser in situ keratomileusis for less than -4.0 to -7.0 diopters of myopia
Restricted heterogeneity of T lymphocytes in combined immunodeficiency with hypereosinophilia (Omenn's syndrome).
The calcium current activated by T cell receptor and store depletion in human lymphocytes is absent in a primary immunodeficiency.