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C R Scriver

Showing results (261-270 of 317) with videos related to

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Pediatrics|June 1, 1983
A perimortem protocol for suspected genetic diseaseJ B Kronick, C R Scriver, P R Goodyer, et al.
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.
Annals of Human Genetics|January 1, 1974
The use of biochemical data in screening for mutant alleles and in genetic counsellingR J Gold, U R Maag, J L Neal, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|October 30, 1973
Quantitative analysis of branched-chain alpha-keto acids as their trimethylsilylated oximesG Lancaster, P Lamm, C R Scriver, 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.
Genetic Epidemiology|January 1, 1992
Specificity and sensitivity of hexosaminidase assays and DNA analysis for the detection of Tay-Sachs disease gene carriers among Ashkenazic JewsM J Fernandes, F Kaplan, C L Clow, et al.
Human Mutation|January 1, 1996
Mutation nomenclature: nicknames, systematic names, and unique identifiersE Beutler, V A McKusick, A G Motulsky, et al.
The New England Journal of Medicine|September 7, 1972
Use of phosphate and vitamin D to prevent dwarfism and rickets in X-linked hypophosphatemiaF H Glorieux, C R Scriver, T M Reade, et al.
Neurology|January 1, 1970
GM1-gangliosidosis without chondrodystrophy or visceromegaly. B-galactosidase deficiency with gangliosidosis and the excessive excretion of a keratan sulfateL S Wolfe, J Callahan, J S Fawcett, 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.
Pageof 32

Showing results (261-270 of 317) with videos related to

Sort By:
Pageof 32
Pediatrics|June 1, 1983
A perimortem protocol for suspected genetic diseaseJ B Kronick, C R Scriver, P R Goodyer, et al.
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.
Annals of Human Genetics|January 1, 1974
The use of biochemical data in screening for mutant alleles and in genetic counsellingR J Gold, U R Maag, J L Neal, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|October 30, 1973
Quantitative analysis of branched-chain alpha-keto acids as their trimethylsilylated oximesG Lancaster, P Lamm, C R Scriver, 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.
Genetic Epidemiology|January 1, 1992
Specificity and sensitivity of hexosaminidase assays and DNA analysis for the detection of Tay-Sachs disease gene carriers among Ashkenazic JewsM J Fernandes, F Kaplan, C L Clow, et al.
Human Mutation|January 1, 1996
Mutation nomenclature: nicknames, systematic names, and unique identifiersE Beutler, V A McKusick, A G Motulsky, et al.
The New England Journal of Medicine|September 7, 1972
Use of phosphate and vitamin D to prevent dwarfism and rickets in X-linked hypophosphatemiaF H Glorieux, C R Scriver, T M Reade, et al.
Neurology|January 1, 1970
GM1-gangliosidosis without chondrodystrophy or visceromegaly. B-galactosidase deficiency with gangliosidosis and the excessive excretion of a keratan sulfateL S Wolfe, J Callahan, J S Fawcett, 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.
Pageof 32