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Diabete & Metabolisme|March 1, 1981
Ammonia metabolism in a family affected by hyperargininemiaI A Qureshi, J Letarte, R Ouellet, et al.
The Journal of Pediatrics|October 1, 1976
TSH measurements from blood spots on filter paper: a confirmatory screening test for neonatal hypothyroidismJ H Dussault, A Parlow, J Letarte, et al.
Science (New York, N.Y.)|May 26, 1978
Genetics and Medicine: an evolving relationshipC R Scriver, C Laberge, C L Clow, et al.
Biochemistry and Cell Biology = Biochimie Et Biologie Cellulaire|May 1, 1986
Purification of mRNA coding for the enzyme deficient in hereditary tyrosinemia, fumarylacetoacetate hydrolaseL M Nicole, J P Valet, C Laberge, et al.
The Journal of Pediatrics|February 1, 1978
Modification of a screening program for neonatal hypothyroidismJ H Dussault, J Morissette, J Letarte, et al.
Cytogenetics and Cell Genetics|January 1, 1990
Localization of the human sex hormone-binding globulin gene (SHBG) to the short arm of chromosome 17 (17p12----p13)D Bérubé, G E Séralini, R Gagné, et al.
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