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2. A DNA-PKcs mutation in a radiosensitive [T.sup.-][B.sup.-] SCID patient inhibits Artemis activation and nonhomologous end-joining

8. Primer immün yetmezlik tanısı alan hasta gruplarında pnömokok serotiplerine karşı antikor cevabının araştırılması

11. A DNA-PKcs mutation in a radiosensitive T–B– SCID patient inhibits Artemis activation and nonhomologous end-joining

16. A Polysplenia-Heterotaxia Case

19. A novel mutation leading to a deletion in the SH3 domain of Bruton's tyrosine kinase.

20. Trimethoprim-sulfamethoxazole induced prolonged hypoglycemia in an infant with MHC class II deficiency: diazoxide as a treatment option.

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