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Clinical Genetics|June 1, 1986
Typing of families with classical phenylketonuria using three alleles of the Hindiii linked restriction fragment polymorphism, detectable with a phenylalanine hydroxylase cDNA probe. Family typing for PKU by linked HindIII RFLPA Speer, H H Dahl, O Riess, et al.Human Genetics|September 15, 2000
Rapid FMR1-protein analysis of fetal blood: an enhancement of prenatal diagnosticsN Lambiris, H Peters, R Bollmann, et al.Human Genetics|August 1, 1990
Immunochemical quantification of Cu/Zn superoxide dismutase in prenatal diagnosis of Down's syndromeT Porstmann, R Wietschke, G Cobet, et al.Prenatal Diagnosis|November 1, 1986
Prenatal diagnosis of classical phenylketonuria by linked restriction fragment length polymorphism analysisA Speer, R Bollman, A Michel, et al.Kinderarztliche Praxis|December 1, 1989
[A staged plan for laboratory diagnosis of hereditary metabolic diseases]H Zöllner, W Tittelbach-Helmrich, N Bannert, et al.Pageof 2