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C R Scriver

Showing results (311-320 of 317) with videos related to

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Pediatric Neurology|October 1, 1994
Cerebral dysgenesis and lactic acidemia: an MRI/MRS phenotype associated with pyruvate dehydrogenase deficiencyM I Shevell, P M Matthews, C R Scriver, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
3-Methylglutaconic aciduria: a marker for as yet unspecified disorders and the relevance of prenatal diagnosis in a 'new' type ('type 4')D Chitayat, J Chemke, K M Gibson, et al.
CMAJ : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne|May 1, 1987
Feasibility of chemical screening of urine for neuroblastoma case finding in infancy in QuebecC R Scriver, D Gregory, M Bernstein, et al.
Brain : a Journal of Neurology|June 1, 1994
Pyruvate dehydrogenase deficiency. Clinical presentation and molecular genetic characterization of five new patientsP M Matthews, R M Brown, L J Otero, et al.
American Journal of Human Genetics|January 1, 1995
Recurrence of the R408W mutation in the phenylalanine hydroxylase locus in EuropeansR C Eisensmith, A A Goltsov, C O'Neill, et al.
European Journal of Human Genetics : EJHG|January 1, 1993
A Pst+ polymorphism in the HEXA gene with an unusual geographic distributionF Kaplan, S Kapoor, D Lee, et al.
Human Mutation|December 25, 2007
Recommendations for locus-specific databases and their curationR G H Cotton, A D Auerbach, J S Beckmann, et al.
Pageof 32

Showing results (311-320 of 317) with videos related to

Sort By:
Pageof 32
You have reached the last page of results.This site can display upto 317 results.
Pediatric Neurology|October 1, 1994
Cerebral dysgenesis and lactic acidemia: an MRI/MRS phenotype associated with pyruvate dehydrogenase deficiencyM I Shevell, P M Matthews, C R Scriver, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
3-Methylglutaconic aciduria: a marker for as yet unspecified disorders and the relevance of prenatal diagnosis in a 'new' type ('type 4')D Chitayat, J Chemke, K M Gibson, et al.
CMAJ : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne|May 1, 1987
Feasibility of chemical screening of urine for neuroblastoma case finding in infancy in QuebecC R Scriver, D Gregory, M Bernstein, et al.
Brain : a Journal of Neurology|June 1, 1994
Pyruvate dehydrogenase deficiency. Clinical presentation and molecular genetic characterization of five new patientsP M Matthews, R M Brown, L J Otero, et al.
American Journal of Human Genetics|January 1, 1995
Recurrence of the R408W mutation in the phenylalanine hydroxylase locus in EuropeansR C Eisensmith, A A Goltsov, C O'Neill, et al.
European Journal of Human Genetics : EJHG|January 1, 1993
A Pst+ polymorphism in the HEXA gene with an unusual geographic distributionF Kaplan, S Kapoor, D Lee, et al.
Human Mutation|December 25, 2007
Recommendations for locus-specific databases and their curationR G H Cotton, A D Auerbach, J S Beckmann, et al.
Pageof 32