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

C Haworth

Showing results (111-120 of 143) with videos related to

Pageof 15
Sort By:
The Journal of Pediatrics|June 1, 1991
Primary oxaluria type 2 (L-glyceric aciduria): a rare cause of nephrolithiasis in childrenL E Seargeant, G W deGroot, L A Dilling, et al.
The Journal of Pediatrics|August 1, 1971
Neonatal hypoglycemia: a discussionA Beard, M Cornblath, J Gentz, et al.
Pediatrics|August 1, 1989
Newborn screening for galactosemia: a new method used in ManitobaC R Greenberg, L A Dilling, R Thompson, et al.
Journal of Clinical Pathology|May 1, 1981
Routine bone marrow examination in the management of acute lymphoblastic leukaemia of childhoodC Haworth, A D Heppleston, P H Morris Jones, et al.
Clinical Genetics|March 1, 1997
Two novel mutations in a Canadian family with aspartylglucosaminuria and early outcome post bone marrow transplantationA Laitinen, M Hietala, J C Haworth, et al.
Nature Cell Biology|December 17, 2009
Defects in DNA ligase I trigger PCNA ubiquitylation at Lys 107Sapna Das-Bradoo, Hai Dang Nguyen, Jamie L Wood, et al.
Cancer Detection and Prevention|January 1, 1992
Sister chromatid exchange (SCE) frequency in lymphocytes of patients with colorectal carcinoma treated with razoxaneC M Price, D Hagger, M Evans, et al.
Journal of Virological Methods|November 7, 2000
Design and validation of immunological tests for the detection of Porcine endogenous retrovirus in biological materialsD N Galbraith, H T Kelly, A Dyke, et al.
American Journal of Human Genetics|February 1, 1990
Infantile hypophosphatasia: localization within chromosome region 1p36.1-34 and prenatal diagnosis using linked DNA markersC R Greenberg, J A Evans, S McKendry-Smith, et al.
The New England Journal of Medicine|March 15, 1984
Homocystinuria and megaloblastic anemia responsive to vitamin B12 therapy. An inborn error of metabolism due to a defect in cobalamin metabolismS Schuh, D S Rosenblatt, B A Cooper, et al.
Pageof 15

Showing results (111-120 of 143) with videos related to

Sort By:
Pageof 15
The Journal of Pediatrics|June 1, 1991
Primary oxaluria type 2 (L-glyceric aciduria): a rare cause of nephrolithiasis in childrenL E Seargeant, G W deGroot, L A Dilling, et al.
The Journal of Pediatrics|August 1, 1971
Neonatal hypoglycemia: a discussionA Beard, M Cornblath, J Gentz, et al.
Pediatrics|August 1, 1989
Newborn screening for galactosemia: a new method used in ManitobaC R Greenberg, L A Dilling, R Thompson, et al.
Journal of Clinical Pathology|May 1, 1981
Routine bone marrow examination in the management of acute lymphoblastic leukaemia of childhoodC Haworth, A D Heppleston, P H Morris Jones, et al.
Clinical Genetics|March 1, 1997
Two novel mutations in a Canadian family with aspartylglucosaminuria and early outcome post bone marrow transplantationA Laitinen, M Hietala, J C Haworth, et al.
Nature Cell Biology|December 17, 2009
Defects in DNA ligase I trigger PCNA ubiquitylation at Lys 107Sapna Das-Bradoo, Hai Dang Nguyen, Jamie L Wood, et al.
Cancer Detection and Prevention|January 1, 1992
Sister chromatid exchange (SCE) frequency in lymphocytes of patients with colorectal carcinoma treated with razoxaneC M Price, D Hagger, M Evans, et al.
Journal of Virological Methods|November 7, 2000
Design and validation of immunological tests for the detection of Porcine endogenous retrovirus in biological materialsD N Galbraith, H T Kelly, A Dyke, et al.
American Journal of Human Genetics|February 1, 1990
Infantile hypophosphatasia: localization within chromosome region 1p36.1-34 and prenatal diagnosis using linked DNA markersC R Greenberg, J A Evans, S McKendry-Smith, et al.
The New England Journal of Medicine|March 15, 1984
Homocystinuria and megaloblastic anemia responsive to vitamin B12 therapy. An inborn error of metabolism due to a defect in cobalamin metabolismS Schuh, D S Rosenblatt, B A Cooper, et al.
Pageof 15