Lintner K, Wu Y, Yang Y, Spencer C, Hauptmann G, Hebert L
Front Immunol. 2016; 7:36.
PMID: 26913032
PMC: 4753731.
DOI: 10.3389/fimmu.2016.00036.
Tobian A, Fuller A, Uglik K, Tisch D, Borge P, Benjamin R
Transfusion. 2013; 54(6):1523-9.
PMID: 24251374
PMC: 4026343.
DOI: 10.1111/trf.12498.
Stowell S, Winkler A, Maier C, Arthur C, Smith N, Girard-Pierce K
Clin Dev Immunol. 2012; 2012:307093.
PMID: 23118779
PMC: 3479954.
DOI: 10.1155/2012/307093.
Raum D, Balner H, Petersen B, Alper C
Immunogenetics. 2012; 10(5):455-68.
PMID: 22457919
DOI: 10.1007/BF01572581.
Awdeh Z, Raum D, Glass D, Agnello V, Schur P, JOHNSTON Jr R
J Clin Invest. 1981; 67(2):581-3.
PMID: 7462431
PMC: 370603.
DOI: 10.1172/JCI110070.
Genetic analysis of C4 deficiency.
Awdeh Z, Ochs H, Alper C
J Clin Invest. 1981; 67(1):260-3.
PMID: 7451653
PMC: 371595.
DOI: 10.1172/JCI110021.
The location of C2, C4, and BF relative to HLA-B and HLA-D.
Raum D, Awdeh Z, Glass D, Yunis E, Alper C
Immunogenetics. 1981; 12(5-6):473-83.
PMID: 7216322
DOI: 10.1007/BF01561689.
Genetics of complement C4. Two homoduplication haplotypes C4S C4S and C4F C4F in a family.
Bruun-Petersen G, Lamm L, Jacobsen B, Kristensen T
Hum Genet. 1982; 61(1):36-8.
PMID: 7129423
DOI: 10.1007/BF00291328.
On the significance of C2, C4, and factor B polymorphisms in disease.
Rittner C, Bertrams J
Hum Genet. 1981; 56(3):235-47.
PMID: 7016719
DOI: 10.1007/BF00274674.
BF types and the mode of inheritance of insulin-dependent diabetes mellitus (IDDM).
Raum D, Awdeh Z, Alper C
Immunogenetics. 1981; 12(1-2):59-74.
PMID: 7009418
DOI: 10.1007/BF01561651.
Phenotypic conversion of human erythrocytes by H-Y antigen.
Muller U, MAYEROVA A, Siebers J, Wolf U
Hum Genet. 1980; 56(2):177-81.
PMID: 7005076
DOI: 10.1007/BF00295691.
Family studies of complement C4 and HLA in man.
Bruun-Petersen G, Lamm L, Sorensen I, Buskjaer L, Mortensen J
Hum Genet. 1981; 58(3):260-7.
PMID: 6948763
DOI: 10.1007/BF00294919.
Inherited structural polymorphism of the fourth component of human complement.
Awdeh Z, Alper C
Proc Natl Acad Sci U S A. 1980; 77(6):3576-80.
PMID: 6932037
PMC: 349660.
DOI: 10.1073/pnas.77.6.3576.
Analysis of active and inactive complement C4 complotypes associated with subtypes of HLA-B17 in different racial groups.
ONEILL G, Nerl C, Pollack M
Am J Hum Genet. 1983; 35(2):309-17.
PMID: 6837577
PMC: 1685544.
Genetic control of the antibody response to allotypes of murine C4.
Spinella D, Roper L, Passmore H
Immunogenetics. 1984; 19(1):87-92.
PMID: 6693139
DOI: 10.1007/BF00364479.
Polymorphism of the fourth complement component in the dog and linkage to the DLA system.
Grosse-Wilde H, Doxiadis G, KRUMBACHER K, Kolb H
Immunogenetics. 1983; 18(5):537-40.
PMID: 6642574
DOI: 10.1007/BF00364394.
Human C4 haplotypes with duplicated C4A or C4B.
Raum D, Awdeh Z, Anderson J, Strong L, Granados J, Teran L
Am J Hum Genet. 1984; 36(1):72-9.
PMID: 6607672
PMC: 1684397.
Cloning of a human complement component C4 gene.
Carroll M, Porter R
Proc Natl Acad Sci U S A. 1983; 80(1):264-7.
PMID: 6572000
PMC: 393353.
DOI: 10.1073/pnas.80.1.264.
Inherited incomplete deficiency of the fourth component of complement (C4) determined by a gene not linked to human histocompatibility leukocyte antigens.
Muir W, Hedrick S, Alper C, Ratnoff O, Schacter B, Wisnieski J
J Clin Invest. 1984; 74(4):1509-14.
PMID: 6480834
PMC: 425321.
DOI: 10.1172/JCI111564.
Human C4 polymorphism: pedigree analysis of qualitative, quantitative, and functional parameters as a basis for phenotype interpretations.
Mauff G, Bender K, Giles C, Goldmann S, Opferkuch W, Wachauf B
Hum Genet. 1984; 65(4):362-72.
PMID: 6420328
DOI: 10.1007/BF00291561.