Study of a case of severe congenital primary, non-sex-linked hypogammaglobulinemia of probable genetic origin. Familial survey
North, M.L.; Rodier, L.; Miech, G.; Rivat, L.; Ropartz, C.; Mayer, S.; Waitz, R.
Nouvelle Revue Francaise d'Hematologie 12(1): 101-110
1972
ISSN/ISBN: 0029-4810 PMID: 4262128 Document Number: 49117
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