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Alexander Whitehead, Ellen Solomon, Susan Chambers, Walter Bodmer, Susan POVEYt, George Fey (1982)
Assignment of the structural gene for the third component of human complement to chromosome 19.Proceedings of the National Academy of Sciences of the United States of America, 79 16
N. Migone, J. Feder, H. Cann, B. West, J. Hwang, N. Takahashi, T. Honjo, A. Piazza, L. Cavalli-Sforza (1983)
Multiple DNA fragment polymorphisms associated with immunoglobulin mu chain switch-like regions in man.Proceedings of the National Academy of Sciences of the United States of America, 80 2
K. Davies, J. Jackson, R. Williamson, P. Harper, S. Ball, M. Sarfarazi, L. Meredith, G. Fey (1983)
Linkage analysis of myotonic dystrophy and sequences on chromosome 19 using a cloned complement 3 gene probe.Journal of Medical Genetics, 20
S. Antonarakis, C. Boehm, P. Giardina, H. Kazazian (1982)
Nonrandom association of polymorphic restriction sites in the beta-globin gene cluster.Proceedings of the National Academy of Sciences of the United States of America, 79 1
C. Langley, E. Montgomery, W. Quattlebaum (1982)
Restriction map variation in the Adh region of Drosophila.Proceedings of the National Academy of Sciences of the United States of America, 79 18
N. Bech‐Hansen, P. Linsley, D. Cox (1983)
Restriction fragment length polymorphisms associated with immunoglobulin C gamma genes reveal linkage disequilibrium and genomic organization.Proceedings of the National Academy of Sciences of the United States of America, 80 22
N. Takahashi, J. Neel, C. Satoh, J. Nishizaki, N. Masunari (1982)
A phylogeny for the principal alleles of the human phosphoglucomutase-1 locus.Proceedings of the National Academy of Sciences of the United States of America, 79 21
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The use of polymorphic DNA and protein markers for the third complement component for determining linkage of familial hypercholesterolaemia.Atherosclerosis, 52 3
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A cloned complement 3 gene probe for linkage analysis of myotonic dystrophy and sequences on chromosome 19. d
R. Scozzari, G. Trippa, A. Santachiara‐Benerecetti, L. Terrenato, C. Iodice, A. Benincasa (1981)
Further genetic heterogeneity of human red cell phosphoglucomutase‐1: a non‐electrophoretic polymorphismAnnals of Human Genetics, 45
Summary Haplotypes have been determined for alleles at two separate polymorphic sites within the human structural gene for complement component 3, identified as a protein polymorphism and as a restriction fragment length polymorphism by hybridization using a cloned gene probe. No evidence was found for appreciable disequilibrium between alleles at these sites, despite their very close linkage.
Annals of Human Genetics – Wiley
Published: Jul 1, 1984
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