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1.
Chronic granulomatous disease in Morocco: genetic, immunological, and clinical features of 12 patients from 10 kindreds.
J Clin Immunol
; 34(4): 452-8, 2014 May.
Article
in English
| MEDLINE | ID: mdl-24596025
2.
The 752delG26 mutation in the RFXANK gene associated with major histocompatibility complex class II deficiency: evidence for a founder effect in the Moroccan population.
Eur J Pediatr
; 169(9): 1069-74, 2010 Sep.
Article
in English
| MEDLINE | ID: mdl-20414676
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