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Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|August 1, 1990
[Analysis of alpha 1-antitrypsin deficiency using DNA methods]U Wick, P Kühnl, W EngelClinical Genetics|April 1, 1995
Restriction fragment length polymorphisms at the apoprotein genes AI, CIII and B-100 and in the 5' flanking region of the insulin gene as possible markers of coronary heart diseaseU Wick, E Witt, W EngelZeitschrift Fur Rechtsmedizin. Journal of Legal Medicine|January 1, 1983
[Blood group expert evaluation: relation between the extent of testing and the reliability of paternity determination. Reflections on revision and guidelines]W Spielmann, P KühnlHuman Genetics|July 12, 1978
Investigations on the PGMa1 polymorphism (phosphoglucomutase--EC 2.7.5.1) by isoelectric focusingP Kühnl, W SpielmannHuman Genetics|January 1, 1979
A third common allele in the transferrin system, TfC3, detected by isoelectric focusingP Kühnl, W SpielmannHuman Genetics|January 1, 1979
PiT: a new allele in the alpha 1-antitrypsin systemP Kühnl, W SpielmannZeitschrift Fur Rechtsmedizin. Journal of Legal Medicine|May 29, 1978
Properdin factor b-polymorphism in the population of Hessen, GermanyP Kühnl, W SpielmannWiener Klinische Wochenschrift|November 7, 1980
[Blood group expertises including related presumptive fathers (author's transl)]W Spielmann, P KühnlBlut|November 1, 1982
Improved coagulation factor XIII B (FXIIIB) phenotyping after neuraminidase treatment of plasma and first description of the FXIIIB 2 phenotypeP Kreckel, P KühnlInfusionstherapie Und Transfusionsmedizin|June 1, 1993
[HIV antigen test of blood donors]B Knödler, P KühnlPageof 43