A modified automated fluorometric method for tyrosine determination in blood spotted on paper: a mass screening procedure for tyrosinemia.
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Amino Acid Metabolism, Inborn Errors↗
Biomedical subjects
C Laberge
Publications and source records attributed to C Laberge.
Genetics of French-Canadians.
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Amino Acid Metabolism, Inborn Errors↗
[In vitro study of hepatic adenyl cyclase in cases of hereditary tyrosinemia].
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Adenosine Triphosphate↗
[Detection of hereditary metabolic diseases in Quebec].
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Amino Acid Metabolism, Inborn Errors↗
[Effects of methionine poisoning on energy metabolism in the guinea pig liver].
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Adenosine Diphosphate↗
[Cytological aspect and intranuclear localization of the heterochromatic segments of C9 chromosomes in man].
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Blood Cells↗
On the application of knowledge to the patient with genetic disease.
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Attitude to Health↗
[Morquio's disease in the province of Quebec].
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Adolescent↗
Rapid method for screening for galactosemia and galactokinase deficiency by measuring galactose in whole blood spotted on paper.
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Autoanalysis↗
[Thyroxine (T4) determination by radioimmunological method in dried blood eluate: new diagnostic method of neonatal hypothyroidism?].
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Analysis of Variance↗
Specific cytological recognition of the heterochromatic segment of number 9 chromosome in man.
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Autoradiography↗
Interphase association of human "Y body" with nucleolus.
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Bone Marrow Cells↗
Differential staining patterns of heterochromatin in man.
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Chromosomes↗
Morphology of the fluorescent interphase body demonstrated by quinacrine in man.
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Chromosomes↗
Quinacrine mustard staining solves the length variations of the human Y chromosome.
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Acridines↗
[Dermatoglyphic studies of French Canadian mongoloids].
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Dermatoglyphics↗
The Quebec Network of Genetic Medicine.
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Chromosome Aberrations↗