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B M Rouse

Showing results (1-10 of 9) with videos related to

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The Journal of Pediatrics|September 1, 1983
Mesodermal origin of axial dysraphismJ W Ferguson, B M Rouse, L Lockhart
Clinical Genetics|May 1, 1984
Ocular, cerebral and cutaneous malformations: confirmation of an associationJ W Ferguson, H T Hutchison, B M Rouse
Biochemical Medicine|October 1, 1981
An enzymatic assay of plasma phenylalanine and tyrosine for the detection and management of phenylketonuriaR S Shen, C J Richardson, B M Rouse, et al.
Clinical Genetics|March 1, 1986
Proximal duplications of chromosome 15: clinical dilemmasO J Hood, B M Rouse, L H Lockhart, et al.
Cancer Genetics and Cytogenetics|November 1, 1990
A complex chromosomal rearrangement and congenital anomalies in the progeny of a mother treated for childhood leukemiaJ L McCombs, C W Daeschner, L H Lockhart, et al.
Journal of the American Dietetic Association|April 1, 1973
Clinical nutrition applications of space food technologyN D Heidelbaugh, M C Smith, P C Rambaut, et al.
American Journal of Human Genetics|July 1, 1996
Phenylalanine hydroxylase gene mutations in the United States: report from the Maternal PKU Collaborative StudyP Guldberg, H L Levy, W B Hanley, et al.
Pediatrics|August 3, 1999
Relationship among genotype, biochemical phenotype, and cognitive performance in females with phenylalanine hydroxylase deficiency: report from the Maternal Phenylketonuria Collaborative StudyF Güttler, C Azen, P Guldberg, et al.
Pediatric Research|May 1, 2001
Congenital heart disease in maternal phenylketonuria: report from the Maternal PKU Collaborative StudyH L Levy, P Guldberg, F Güttler, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
The Journal of Pediatrics|September 1, 1983
Mesodermal origin of axial dysraphismJ W Ferguson, B M Rouse, L Lockhart
Clinical Genetics|May 1, 1984
Ocular, cerebral and cutaneous malformations: confirmation of an associationJ W Ferguson, H T Hutchison, B M Rouse
Biochemical Medicine|October 1, 1981
An enzymatic assay of plasma phenylalanine and tyrosine for the detection and management of phenylketonuriaR S Shen, C J Richardson, B M Rouse, et al.
Clinical Genetics|March 1, 1986
Proximal duplications of chromosome 15: clinical dilemmasO J Hood, B M Rouse, L H Lockhart, et al.
Cancer Genetics and Cytogenetics|November 1, 1990
A complex chromosomal rearrangement and congenital anomalies in the progeny of a mother treated for childhood leukemiaJ L McCombs, C W Daeschner, L H Lockhart, et al.
Journal of the American Dietetic Association|April 1, 1973
Clinical nutrition applications of space food technologyN D Heidelbaugh, M C Smith, P C Rambaut, et al.
American Journal of Human Genetics|July 1, 1996
Phenylalanine hydroxylase gene mutations in the United States: report from the Maternal PKU Collaborative StudyP Guldberg, H L Levy, W B Hanley, et al.
Pediatrics|August 3, 1999
Relationship among genotype, biochemical phenotype, and cognitive performance in females with phenylalanine hydroxylase deficiency: report from the Maternal Phenylketonuria Collaborative StudyF Güttler, C Azen, P Guldberg, et al.
Pediatric Research|May 1, 2001
Congenital heart disease in maternal phenylketonuria: report from the Maternal PKU Collaborative StudyH L Levy, P Guldberg, F Güttler, et al.
Pageof 1