By Prof. Dr. Wolfgang Dahr, John Moulds, Phyllis Unger, Dominique Blanchard (auth.), Prof. Dr. med. B. Brinkmann, Dr. med. Klavs Henningsen (eds.)
Read Online or Download 11th Congress of the Society for Forensic Haemogenetics (Gesellschaft für forensische Blutgruppenkunde e.V.): Copenhagen, August 6–10, 1985 PDF
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Additional info for 11th Congress of the Society for Forensic Haemogenetics (Gesellschaft für forensische Blutgruppenkunde e.V.): Copenhagen, August 6–10, 1985
As part of Immediate post-mortem care. deceased persons should be Identified as belonging to one of the above three groups (AIDS. ARC. Individuals with epidemiologic risk) and Identification should remain with the body 2. The procedures followed before. Personnel Involved In performing an autopsy should wear double gloves •. masks. protective eyewear. gowns. waterproof aprons and shoe coverings. Contaminated Instruments and surfaces should be handled as Infective 3. Appropriate precautions to prevent parenteral or mucousmembrane exposure of personnel to body fluids should be evaluated The biosafety guidelines for use of HTLV-III and related viruses mention the accidental parenteral self-inoculation, droplet exposure to mucous membranes by splashing or spraying of infectious materials (possibly also aerosols), contact exposure of broken skin as well as pricking, puncturing, cutting of skin with scalpels or other sharp objects like broken glassware.
These multiple loci, coding for similar though structurally distinct polypeptides have mostly arisen as a result of gene duplication during the course of evolution and the duplicate genes have subsequently diverged in structure as a result of point mutation. In many cases the polypeptides coded by each of the loci are synthesised together in the same cell but there are often marked disparities in the rates of synthesis in different tissues and at different stages of development. Such differences are important in forensic analysis since they may be used as indicators of the species and tissue of origin of an unknown biological stain or other types of sample and in some cases may also give an indication as to whether the specimen was derived from an adult or an infant.
Mayr WR: HLA-DR in der Paternitatsbegutachtung. Referate 10. into Tagung Ges. f. forens. Blutgruppenkunde, MUnchen. 1983. s. 41 Amniotic fluid cell and chorionic villi culture for prenatal HLA-determination. Lars O. Vejerslev, Hanna E. Hansen, Jes G. Westergaard & Finn S0ndergaard. Kennedy Institute, Glostrup, Copenhagen. University Institute of Forensic Genetics, Copenhagen. Department of Obstetrics and Gynecology, Odense University Hospital, Odense, Denmark. Department of Obstetrics and Gynecology, Copenhagen Municipal Hospital in Hvidovre, Copenhagen, Denmark.