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Human Genetics|January 28, 1976
On the population genetics of phenylketonuria in the G.D.RG Machill, A KnappHuman Genetics|January 1, 1983
Reliability of the Tønnesen technique for the identification of Hunter carriersL Petruschka, G Machill, M Wehnert, et al.Zentralblatt Fur Gynakologie|January 1, 1975
[Prenatal brain damage in maternal, untreated phenylketonuria]W H Peters, H Lubs, G Machill, et al.Acta Biologica Et Medica Germanica|January 1, 1975
[Determination of kynureninase activity in oligophrenic children with hereditary taint, before and after vitamin B6 treatment]U Grimm, A Knapp, G Machill, et al.European Journal of Pediatrics|March 1, 1990
Birth distribution in cystic fibrosis and phenylketonuriaG Machill, J Gedschold, S KropfJournal of Medical Genetics|June 1, 1991
Segregation and sporadic cases in families with Hunter's syndromeG Machill, G Barbujani, G A Danieli, et al.American Journal of Hospital Pharmacy|November 1, 1979
Strategy for increasing the demand for clinical pharmacistsD A Knapp, D A KnappZeitschrift Fur Die Gesamte Innere Medizin Und Ihre Grenzgebiete|June 1, 1981
[Porphyrin diseases with particular emphasis on hereditary]A KnappTissue Antigens|February 26, 2005
Denaturing gradient gel electrophoresis and its use in the detection of major histocompatibility complex polymorphismL A KnappPageof 40