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By Dekker J.   de Boer M.   Roos D.  

Experimental Hematology, Vol. 29, Iss. 11, 2001-11 ,pp. : 1319-1325

Elsevier

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Genomic Structure of the Human p47-phox (NCF1) Gene

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Severe phenotype of chronic granulomatous disease presenting in a female with a de novo mutation in gp91-phox and a non familial, extremely skewed X chromosome inactivation

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Utility of Screening for Chronic Granulomatous Disease in Patients with Inflammatory Bowel Disease

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Clinical Immunology, Vol. 105, Iss. 3, 2002-12 ,pp. : 273-278

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