Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

E R McCabe

Showing results (121-130 of 160) with videos related to

Pageof 16
Sort By:
Molecular Genetics and Metabolism|January 4, 2001
Midkine is expressed early in rat fetal adrenal developmentP Dewing, S T Ching, Y H Zhang, et al.
The Journal of Pediatrics|October 1, 1978
Homotransplantation of the liver in a patient with hepatoma and hereditary tyrosinemiaR O Fisch, E R McCabe, D Doeden, et al.
European Journal of Pediatrics|November 1, 1987
Infantile glycerol kinase deficiency--a condition requiring prompt identification. Clinical, biochemical, and morphological findings in two casesA Kohlschütter, H P Willig, D Schlamp, et al.
The Journal of Pediatrics|December 1, 1980
Neutropenia in a patient with type IB glycogen storage disease: in vitro response to lithium chlorideE R McCabe, T R Melvin, D O'Brien, et al.
Journal of Inherited Metabolic Disease|January 1, 1989
The management of breast feeding among infants with phenylketonuriaL McCabe, A E Ernest, M R Neifert, et al.
American Journal of Human Genetics|November 1, 1990
Deletion mapping of Aland Island eye disease to Xp21 between DXS67 (B24) and Duchenne muscular dystrophyD A Pillers, J A Towbin, J S Chamberlain, et al.
JPEN. Journal of Parenteral and Enteral Nutrition|September 1, 1981
Zinc and copper status of treated children with phenylketonuriaP B Acosta, P M Fernhoff, H S Warshaw, et al.
Gene|October 31, 1996
Ahch, the mouse homologue of DAX1: cloning, characterization and synteny with GyK, the glycerol kinase locusW Guo, R S Lovell, Y H Zhang, et al.
Journal of Inherited Metabolic Disease|January 1, 1982
Zinc status and growth of children undergoing treatment for phenylketonuriaP B Acosta, P M Fernhoff, H S Warshaw, et al.
Community Genetics|February 13, 2004
Integrating genetic services into public health--guidance for state and territorial programs from the National Newborn Screening and Genetics Resource Center (NNSGRC)C I Kaye, R Laxova, J E Livingston, et al.
Pageof 16

Showing results (121-130 of 160) with videos related to

Sort By:
Pageof 16
Molecular Genetics and Metabolism|January 4, 2001
Midkine is expressed early in rat fetal adrenal developmentP Dewing, S T Ching, Y H Zhang, et al.
The Journal of Pediatrics|October 1, 1978
Homotransplantation of the liver in a patient with hepatoma and hereditary tyrosinemiaR O Fisch, E R McCabe, D Doeden, et al.
European Journal of Pediatrics|November 1, 1987
Infantile glycerol kinase deficiency--a condition requiring prompt identification. Clinical, biochemical, and morphological findings in two casesA Kohlschütter, H P Willig, D Schlamp, et al.
The Journal of Pediatrics|December 1, 1980
Neutropenia in a patient with type IB glycogen storage disease: in vitro response to lithium chlorideE R McCabe, T R Melvin, D O'Brien, et al.
Journal of Inherited Metabolic Disease|January 1, 1989
The management of breast feeding among infants with phenylketonuriaL McCabe, A E Ernest, M R Neifert, et al.
American Journal of Human Genetics|November 1, 1990
Deletion mapping of Aland Island eye disease to Xp21 between DXS67 (B24) and Duchenne muscular dystrophyD A Pillers, J A Towbin, J S Chamberlain, et al.
JPEN. Journal of Parenteral and Enteral Nutrition|September 1, 1981
Zinc and copper status of treated children with phenylketonuriaP B Acosta, P M Fernhoff, H S Warshaw, et al.
Gene|October 31, 1996
Ahch, the mouse homologue of DAX1: cloning, characterization and synteny with GyK, the glycerol kinase locusW Guo, R S Lovell, Y H Zhang, et al.
Journal of Inherited Metabolic Disease|January 1, 1982
Zinc status and growth of children undergoing treatment for phenylketonuriaP B Acosta, P M Fernhoff, H S Warshaw, et al.
Community Genetics|February 13, 2004
Integrating genetic services into public health--guidance for state and territorial programs from the National Newborn Screening and Genetics Resource Center (NNSGRC)C I Kaye, R Laxova, J E Livingston, et al.
Pageof 16