Another family with a silent allele of properdin factor B polymorphism (BF*QO)-Reference-Cited by-同舟云学术

Another family with a silent allele of properdin factor B polymorphism (BF*QO)

Published:1985-08 Issue:4 Volume:70 Page:321-323
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Bertrams J.,Mauff G.

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/BF00295369.pdf

Reference14 articles.

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2. Awdeh ZL, Raum D, Yunis EJ, Alper CA (1983) Extended HLA-complement-glyoxalase allele haplotype: Evidence for Tt-like complex in man. Proc Natl Acad Sci USA 80:259?263

3. Dewald G, Rittner Ch (1980) Polymorphism of the second component of human complement: Observation of the rare phenotype C2 (C2B) and data on the localization of the C2 locus in the HLA region. Vox Sang 37:47?54

4. K�mpf J, Bissbort S, Gussmann S, Ritter H (1975) Polymorphism of red cell glyoxalase I (E.C.: 4.41I). A new genetic marker in man. Humangenetik 27:141?143

5. Lachmann PJ (1984) Inherited complement deficiencies. Philos Trans R Soc Lond [Biol] 306:419?430

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1. Mice Deficient for the Complement Factor B Develop and Reproduce Normally;Scandinavian Journal of Immunology;1998-04

2. Indication for a Silent Allele of Properdin Factor B Polymorphism (BF*Q0) in a Paternity Case;16th Congress of the International Society for Forensic Haemogenetics (Internationale Gesellschaft für forensische Hämogenetik e.V.), Santiago de Compostela, 12–16 September 1995;1996

3. Nomenclature for human complement factor B2.;European Journal of Immunogenetics;1993-08

4. Nomenclature for human complement factor B;Journal of Immunological Methods;1993-07

5. Genetic Deficiencies of the Complement System and Association with Disease-Early Components;International Reviews of Immunology;1993-01