C R Scriver|C L Clow - JoVE Visualize

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Genetic Counseling (Geneva, Switzerland)|January 1, 1990

Fertility in couples heterozygous for the tyrosinemia gene in Saguenay Lac-St-JeanM De Braekeleer, V Lamarre, C R Scriver, et al.

Canadian Anaesthetists' Society Journal|May 1, 1982

Effect of nitrous oxide anaesthesia on homocystine excretionJ C Bevan, D S Rosenblatt, C L Clow, et al.

Pediatric Neurology|May 1, 1994

Magnetic resonance spectroscopy in Niemann-Pick disease type C: correlation with diagnosis and clinical response to cholestyramine and lovastatinM Sylvain, D L Arnold, C R Scriver, et al.

Prenatal Diagnosis|July 1, 1997

Prenatal diagnosis for inborn errors of metabolism and haemoglobinopathies: the Montreal Children's Hospital experienceK Sasi, D Sanderson, P Eydoux, et al.

Journal of Inherited Metabolic Disease|January 1, 1992

Hereditary tyrosinaemia type II in a consanguineous Ashkenazi Jewish family: intrafamilial variation in phenotype; absence of parental phenotype effects on the fetusD Chitayat, A Balbul, V Hani, et al.

American Journal of Medical Genetics|May 1, 1990

Identification of deletion and triple alpha-globin gene haplotypes in the Montreal beta-thalassemia screening program: implications for genetic medicineB R Akerman, T M Fujiwara, G A Lancaster, et al.

American Journal of Human Genetics|December 18, 1997

Human phenylalanine hydroxylase mutations and hyperphenylalaninemia phenotypes: a metanalysis of genotype-phenotype correlationsE Kayaalp, E Treacy, P J Waters, et al.

The Journal of Pediatrics|November 1, 1987

Nephrocalcinosis and its relationship to treatment of hereditary ricketsP R Goodyer, J B Kronick, S Jequier, et al.

Journal of Inherited Metabolic Disease|January 1, 1983

Histidinaemia. Part III: Impact; a prospective studyJ T Coulombe, B L Kammerer, H L Levy, et al.

Proceedings of the National Academy of Sciences of the United States of America|October 1, 1980

Cord-blood tyrosine levels in the full-term phenylketonuric fetus and the "justification hypothesis"C R Scriver, D E Cole, S A Houghton, et al.

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Showing results (141-150 of 175) with videos related to

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Pageof 18

Genetic Counseling (Geneva, Switzerland)|January 1, 1990

Fertility in couples heterozygous for the tyrosinemia gene in Saguenay Lac-St-JeanM De Braekeleer, V Lamarre, C R Scriver, et al.

Canadian Anaesthetists' Society Journal|May 1, 1982

Effect of nitrous oxide anaesthesia on homocystine excretionJ C Bevan, D S Rosenblatt, C L Clow, et al.

Pediatric Neurology|May 1, 1994

Magnetic resonance spectroscopy in Niemann-Pick disease type C: correlation with diagnosis and clinical response to cholestyramine and lovastatinM Sylvain, D L Arnold, C R Scriver, et al.

Prenatal Diagnosis|July 1, 1997

Prenatal diagnosis for inborn errors of metabolism and haemoglobinopathies: the Montreal Children's Hospital experienceK Sasi, D Sanderson, P Eydoux, et al.

Journal of Inherited Metabolic Disease|January 1, 1992

Hereditary tyrosinaemia type II in a consanguineous Ashkenazi Jewish family: intrafamilial variation in phenotype; absence of parental phenotype effects on the fetusD Chitayat, A Balbul, V Hani, et al.

American Journal of Medical Genetics|May 1, 1990

Identification of deletion and triple alpha-globin gene haplotypes in the Montreal beta-thalassemia screening program: implications for genetic medicineB R Akerman, T M Fujiwara, G A Lancaster, et al.

American Journal of Human Genetics|December 18, 1997

Human phenylalanine hydroxylase mutations and hyperphenylalaninemia phenotypes: a metanalysis of genotype-phenotype correlationsE Kayaalp, E Treacy, P J Waters, et al.

The Journal of Pediatrics|November 1, 1987

Nephrocalcinosis and its relationship to treatment of hereditary ricketsP R Goodyer, J B Kronick, S Jequier, et al.

Journal of Inherited Metabolic Disease|January 1, 1983

Histidinaemia. Part III: Impact; a prospective studyJ T Coulombe, B L Kammerer, H L Levy, et al.

Proceedings of the National Academy of Sciences of the United States of America|October 1, 1980

Cord-blood tyrosine levels in the full-term phenylketonuric fetus and the "justification hypothesis"C R Scriver, D E Cole, S A Houghton, et al.

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