Citation: C. Rittner et B. Stradmannbellinghausen, HUMAN-COMPLEMENT C81 (C8 A) POLYMORPHISM - DETECTION AND SEGREGATION OF NEW VARIANTS, Human genetics, 92(4), 1993, pp. 413-416
Citation: T. Kaufmann et al., THE HUMAN-COMPLEMENT COMPONENT C8B GENE - STRUCTURE AND PHYLOGENETIC RELATIONSHIP, Human genetics, 92(1), 1993, pp. 69-75
Authors:
ZHANG L
STRADMANNBELLINGHAUSEN B
SCHNEIDER PM
RITTNER C
Citation: L. Zhang et al., GENETIC POLYMORPHISMS OF THE A AND B SUBUNITS OF COAGULATION FACTOR-XIII IN THE CHINESE POPULATION, Experimental and clinical immunogenetics, 10(3), 1993, pp. 137-140
Authors:
YAO Z
HARTUNG K
EHRFELD H
SEELIG HP
DEICHER HG
BRUNNLER G
KELLER E
ALBERT E
BAUR M
CORVETTA A
FREY J
KALDEN JR
KRAPF F
LAKOMEK HJ
LANG B
DELANGE GG
PETER HH
PIRNER H
RITTNER C
ROTHER E
SCHNEIDER P
SEUCHTER S
SPATH P
SPECKER C
STANGEL W
Citation: Z. Yao et al., NO DIRECT CORRELATION BETWEEN HLA-DPB1 AND ANTIBODIES AGAINST RECOMBINANT RO (SS-A) LA(SS-B) PROTEINS IN SYSTEMIC LUPUS-ERYTHEMATOSUS/, Rheumatology international, 13(4), 1993, pp. 155-158
Authors:
KAZATCHKINE MD
HAUPTMANN G
ABBAL M
ALPER CA
ARNOLD D
CHRISTIANSEN F
DAWKINS RL
DOXIADIS G
GESERICK G
GILES CM
HOBART M
JAHN I
LOKKI ML
MAUFF G
NAKAMURA S
ONEILL GJ
RITTNER C
SCHNEIDER PM
SEGURADO OG
SIEMENS I
SUZUKI K
TOKUNAGA K
URINGLAMBERT B
Citation: Md. Kazatchkine et al., IMMUNOLOGICAL STANDARDIZATION - NOMENCLATURE FOR HUMAN-COMPLEMENT COMPONENT C2 (REPRINTED FROM BULL WHO, VOL 70, PG 527-528, 1992), Journal of immunological methods, 163(1), 1993, pp. 1-2
Authors:
KAZATCHKINE M
MAUFF G
ABBAL M
ALPER CA
CHRISTIANSEN F
CUCCIA M
DAWKINS R
DOXIADIS G
DUTOIT E
GILES C
GESERICK G
HAUPTMANN G
HOBART M
LOKKI M
MCLEAN R
NAKAMURA S
ONEILL G
PARTANEN J
RITTNER C
SCHNEIDER PM
SEGURADO O
SIEMENS J
SUZUKI K
DEMESSIAS IT
Citation: M. Kazatchkine et al., IMMUNOLOGICAL STANDARDIZATION - REVISED NOMENCLATURE FOR HUMAN-COMPLEMENT COMPONENT C4 (REPRINTED FROM BULL WHO, VOL 70, PG 531-535, 1992), Journal of immunological methods, 163(1), 1993, pp. 3-7
Citation: G. Barba et al., GENETIC-BASIS OF HUMAN-COMPLEMENT C4A DEFICIENCY - DETECTION OF A POINT MUTATION LEADING TO NONEXPRESSION, The Journal of clinical investigation, 91(4), 1993, pp. 1681-1686