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E R McCabe

Showing results (71-80 of 160) with videos related to

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The New England Journal of Medicine|May 21, 1981
Screening for phenylketonuriaN A Holtzman, E R McCabe, G C Cunningham, et al.
The Journal of Pediatrics|August 26, 1998
Minipuberty of infancy and adolescent pubertal function in adrenal hypoplasia congenitaK B Kaiserman, J M Nakamoto, M E Geffner, et al.
Human Genetics|March 1, 1987
DNA microextraction from dried blood spots on filter paper blotters: potential applications to newborn screeningE R McCabe, S Z Huang, W K Seltzer, et al.
Analytical Biochemistry|June 1, 1974
Separation and automated analysis of phosphorylated metabolic intermediatesS P Bessman, P J Geiger, T C Lu, et al.
Pediatrician|January 1, 1983
The use of insulin pump therapy in adolescentsG J Klingensmith, B P Giordano, E R McCabe, et al.
Human Genetics|August 1, 1991
Isodicentric X chromosome in a patient with Turner syndrome--implications for localization of the X-inactivation centerA L Pettigrew, E R McCabe, F F Elder, et al.
Molecular Genetics and Metabolism|June 28, 2000
Fructose-1,6-diphosphatase deficiency and glyceroluria: one possible etiology for GISM E Beatty, Y H Zhang, E R McCabe, et al.
Journal of Pediatric Gastroenterology and Nutrition|February 1, 1989
Pitfalls in diagnosing galactosemia: false negative newborn screening following red blood cell transfusionR J Sokol, E R McCabe, A M Kotzer, et al.
American Journal of Human Genetics|December 1, 1992
Xp21 contiguous gene syndromes: deletion quantitation with bivariate flow karyotyping allows mapping of patient breakpointsE R McCabe, J A Towbin, G van den Engh, et al.
Child Development|December 1, 1990
Neuropsychology of early-treated phenylketonuria: specific executive function deficitsM C Welsh, B F Pennington, S Ozonoff, et al.
Pageof 16

Showing results (71-80 of 160) with videos related to

Sort By:
Pageof 16
The New England Journal of Medicine|May 21, 1981
Screening for phenylketonuriaN A Holtzman, E R McCabe, G C Cunningham, et al.
The Journal of Pediatrics|August 26, 1998
Minipuberty of infancy and adolescent pubertal function in adrenal hypoplasia congenitaK B Kaiserman, J M Nakamoto, M E Geffner, et al.
Human Genetics|March 1, 1987
DNA microextraction from dried blood spots on filter paper blotters: potential applications to newborn screeningE R McCabe, S Z Huang, W K Seltzer, et al.
Analytical Biochemistry|June 1, 1974
Separation and automated analysis of phosphorylated metabolic intermediatesS P Bessman, P J Geiger, T C Lu, et al.
Pediatrician|January 1, 1983
The use of insulin pump therapy in adolescentsG J Klingensmith, B P Giordano, E R McCabe, et al.
Human Genetics|August 1, 1991
Isodicentric X chromosome in a patient with Turner syndrome--implications for localization of the X-inactivation centerA L Pettigrew, E R McCabe, F F Elder, et al.
Molecular Genetics and Metabolism|June 28, 2000
Fructose-1,6-diphosphatase deficiency and glyceroluria: one possible etiology for GISM E Beatty, Y H Zhang, E R McCabe, et al.
Journal of Pediatric Gastroenterology and Nutrition|February 1, 1989
Pitfalls in diagnosing galactosemia: false negative newborn screening following red blood cell transfusionR J Sokol, E R McCabe, A M Kotzer, et al.
American Journal of Human Genetics|December 1, 1992
Xp21 contiguous gene syndromes: deletion quantitation with bivariate flow karyotyping allows mapping of patient breakpointsE R McCabe, J A Towbin, G van den Engh, et al.
Child Development|December 1, 1990
Neuropsychology of early-treated phenylketonuria: specific executive function deficitsM C Welsh, B F Pennington, S Ozonoff, et al.
Pageof 16