Unusual sialilation of three different rare genetic variants of serum DBP: Gc1A17, Gc1A16, and Gc1A11THYMANN, M; HOSTE, B; SCHEFFRAHN, W et al.Human genetics. 1985, Vol 69, Num 3, pp 224-227, issn 0340-6717Article

Distribution of Gc subtypes in Aragon (North-East spain)MARTINEZ-JARRETA, B; CASTELLANO, M; CRIADO, M. T et al.Human heredity. 1989, Vol 39, Num 1, pp 46-48, issn 0001-5652, 3 p.Article

A Gc silent allele encountered in a paternity caseSUZUKI, K; ITOH, S; KAWAI, N et al.Human heredity. 1986, Vol 36, Num 5, pp 326-329, issn 0001-5652Article

Gc and Tf subtypes in GreeceKOUVATSI, A; TRIANTAPHYLLIDIS, C. D.Human heredity. 1987, Vol 37, Num 1, pp 62-64, issn 0001-5652Article

Close linkage of MT2Pl with GC on chromosome 4PAKSTIS, A. J; KIDD, J. R; CASTIGLIONE, C et al.Cytogenetics and cell genetics. 1986, Vol 41, Num 3, pp 189-190, issn 0301-0171Article

Evidence against linkage of the gene for usher's syndrome type 1 with group specific component (GC) on chromosome 4BONNEAU, D; KAPLAN, J; BERTHIER, M et al.Annales de génétique (Paris). 1990, Vol 33, Num 2, pp 103-104, issn 0003-3995, 2 p.Article

Gc and C3 polymorphisms in Central SardiniaGRUPPIONI, G; LUNESU, M; SUCCA, V et al.Human heredity. 1988, Vol 38, Num 3, pp 178-179, issn 0001-5652Article

Group-specific component (Gc) subtypes in the indian subcontinentPAPIHA, S. S; WHITE, I; SINGH, B. N et al.Human heredity. 1987, Vol 37, Num 4, pp 250-254, issn 0001-5652Article

Ethnic variation in vitamin D-binding protein (GC): a review of isoelectric focusing studies in human populationsKAMBOH, M. I; FERRELL, R. E.Human genetics. 1986, Vol 72, Num 4, pp 281-293, issn 0340-6717Article

Heterogeneity in disease associationsMAYO, O; STREET, D. J.Human heredity. 1986, Vol 36, Num 2, pp 89-92, issn 0001-5652Article

Serum protein polymorphisms in patients with primary Sjögren's syndromeMITCHELL, R. J; FABB, S. A; WHITTINGHAM, S et al.Human heredity. 1985, Vol 35, Num 5, pp 303-305, issn 0001-5652Article

Increased turnover of Gc-Globulin in patients with hepatic encephalopathySCHIØDT, F. V; CLEMMESEN, J. O; BONDESEN, S et al.Scandinavian journal of gastroenterology. 2001, Vol 36, Num 9, pp 998-1003, issn 0036-5521Article

GC subtyping infection in a Spanish population: no evidence of an association between GC subtypes and AIDSALONSO, A; MONTESINO, M; ITURRALDE, M. J et al.Human heredity. 1990, Vol 40, Num 1, pp 34-37, issn 0001-5652Article

Distribution of transferrin and group-specific component subtypes among parsis of IndiaUNDEVIA, J. V; SAHA, N.Human heredity. 1987, Vol 37, Num 4, pp 205-210, issn 0001-5652Article

The effect of Gc genotype on fasting insuling level in Dogrib IndiansSZATHMARY, E. J. E.Human genetics. 1987, Vol 75, Num 4, pp 368-372, issn 0340-6717Article

Antitrypsin and Gc polymorphisms in some populations of Congo: an unusual, highly frequent mutant, PI^S, in Bateke and BabengaPASCALI, V. L; RANALLETTA, D; SPEDINI, G et al.Annals of human biology. 1986, Vol 13, Num 3, pp 267-271, issn 0301-4460Article

On the variability of Gc subtypes in ItalyWALTER, H; KANNAPINN, G; DANNEWITZ, A et al.Human heredity. 1986, Vol 36, Num 1, pp 50-53, issn 0001-5652Article

Serum protein polymorphism among Tunisian Berbers: haptoglobin, transferrin and group-specific component subtypes, C3 and BF typesCHIBANI, J; LEFRANC, G; CONSTANS, J et al.Annals of human biology. 1985, Vol 12, Num 5, pp 449-462, issn 0301-4460Article

A monoclonal antibody against human vitamin-D-binding protein for the analysis of genetic variation in the group-specific component system (Gc)HOFFMANN, R; BRAUN, A; CLEVE, H et al.Human genetics. 1990, Vol 84, Num 2, pp 137-146, issn 0340-6717, 10 p.Article

Serum Gc, Hp and α₂HS phenotypes in human T-lymphotropic leukemia virus type I infectionOGATA, M; IWASAKI, M; KUBO, S.-I et al.Human heredity. 1990, Vol 40, Num 5, pp 253-256, issn 0001-5652Article

Investigations on the variability of haptoglobin, transferrin and Gc polymorphisms in Assam, IndiaWALTER, H; MUKHERJEE, B. N; GILBERT, K et al.Human heredity. 1986, Vol 36, Num 6, pp 388-396, issn 0001-5652Article

Progress toward resolving the possible linkage of multiple endocrine neoplasia type 2A to haptoglobin and group-specific loci: use of restriction fragment length polymorphisms extends exclusion regionKIDD, K. K; KIDD, J. R; CASTIGLIONE, C. M et al.Genetic epidemiology. 1986, Vol 3, Num 3, pp 195-200, issn 0741-0395Article

Serum protein groups in renal cell carcinomaFRÖHLANDER, N; LJUNGBERG, B.Human heredity. 1986, Vol 36, Num 2, pp 119-122, issn 0001-5652Article

Serum protein polymorphism in Bali (Indonesia)CONSTANS, J; GOUAILLARD, C; BREGUET, G et al.Annals of human biology. 1986, Vol 13, Num 6, pp 537-545, issn 0301-4460Article

Group-specific component (Gc) subtypes in Gambian and Transkeian populations: a description of a new variantPAPIHA, S. S; CONSTANS, J; WHITE, I et al.Annals of human biology. 1985, Vol 12, Num 1, pp 17-26, issn 0301-4460Article