Lack of linkage between gene(s) controlling the synthesis of the seventh component of complement and the HLA region on chromosome No. 6 in man

Author:

Rittner Ch.,Opferkuch W.,Wellek B.,Grosse-Wilde H.,Wernet P.

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Reference14 articles.

1. Grosse-Wilde, H., Netzel, B., Mempel, W., Ruppelt, W., Brehm, G., Bertrams, J., Ewald, R., Lenhard, V., Rittner, Ch., Scholz, S., Albert, E. D.: Immunogenetics of LD determinants in man. Histocompatibility testing, F. Kissmeyer-Nielsen, ed., p. 526. Copenhagen: Munksgaard 1975

2. Hannema, A. J., Pondman, K. W., D�hmann, U., Gadner, H., Dorren, I. J.: C7 deficiency in man. In: Protides of the biological fluids, H. Peeters, ed. Oxford: Pergamon 1975

3. K�mpf, J., Bissbort, S., Gussmann, S., Ritter, H.: Polymorphism of red cell glyoxalase I (E.C. 4.4.1.5.). A new genetic marker in man. Humangenetik 27, 141?143 (1975)

4. Martin, W.: Personal communication

5. Mayr, W. R., Mayr, D., K�mpf, J., Bissbort, S., Ritter, H.: Possible linkage of HL-A and GLO. Humangenetik 31, 241?242 (1976)

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