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C Laberge

Showing results (71-80 of 111) with videos related to

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Clinical Chemistry|March 1, 1980
Thyroxine-binding globulin capacity and concentration evaluated from blood spots on filter-paper in a screening program for neonatal hypothyroidismJ H Dussault, J Morissette, J Letarte, 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.
Progress in Medical Genetics|January 1, 1973
On the application of knowledge to the patient with genetic diseaseC L Clow, F C Fraser, C Laberge, et al.
L'Union Medicale Du Canada|April 1, 1980
[Hereditary metabolic diseases in Quebec: blood screening]A Grenier, J Morissette, J H Dussault, et al.
Meat Science|May 29, 2012
"Chilled" pork--Part I: Sensory and physico-chemical qualityT M Ngapo, L Riendeau, C Laberge, et al.
American Journal of Human Genetics|May 1, 1990
Recurrent mutation, gene conversion, or recombination at the human phenylalanine hydroxylase locus: evidence in French-Canadians and a catalog of mutationsS W John, R Rozen, C R Scriver, et al.
American Journal of Human Genetics|December 1, 1989
Novel PKU mutation on haplotype 2 in French-CanadiansS W John, R Rozen, R Laframboise, et al.
Human Mutation|January 1, 1992
Five mutations at the PAH locus account for almost 90% of PKU mutations in French-Canadians from eastern QuebecS W John, R Rozen, R Laframboise, et al.
Clinical Genetics|September 11, 2002
Sibship stability of genotype and phenotype in myotonic dystrophyD Brisson, M Tremblay, C Prévost, et al.
Pageof 12

Showing results (71-80 of 111) with videos related to

Sort By:
Pageof 12
Clinical Chemistry|March 1, 1980
Thyroxine-binding globulin capacity and concentration evaluated from blood spots on filter-paper in a screening program for neonatal hypothyroidismJ H Dussault, J Morissette, J Letarte, 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.
Progress in Medical Genetics|January 1, 1973
On the application of knowledge to the patient with genetic diseaseC L Clow, F C Fraser, C Laberge, et al.
L'Union Medicale Du Canada|April 1, 1980
[Hereditary metabolic diseases in Quebec: blood screening]A Grenier, J Morissette, J H Dussault, et al.
Meat Science|May 29, 2012
"Chilled" pork--Part I: Sensory and physico-chemical qualityT M Ngapo, L Riendeau, C Laberge, et al.
American Journal of Human Genetics|May 1, 1990
Recurrent mutation, gene conversion, or recombination at the human phenylalanine hydroxylase locus: evidence in French-Canadians and a catalog of mutationsS W John, R Rozen, C R Scriver, et al.
American Journal of Human Genetics|December 1, 1989
Novel PKU mutation on haplotype 2 in French-CanadiansS W John, R Rozen, R Laframboise, et al.
Human Mutation|January 1, 1992
Five mutations at the PAH locus account for almost 90% of PKU mutations in French-Canadians from eastern QuebecS W John, R Rozen, R Laframboise, et al.
Clinical Genetics|September 11, 2002
Sibship stability of genotype and phenotype in myotonic dystrophyD Brisson, M Tremblay, C Prévost, et al.
Pageof 12