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

F Cockburn

Showing results (121-130 of 134) with videos related to

Pageof 14
Sort By:
Lancet (London, England)|January 17, 1976
Hyaline-membrane disease, alkaline buffer treatment, and cerebral intraventricular halphaemorrhageJ M Anderson, A D Bain, J K Brown, et al.
Lancet (London, England)|February 21, 1976
Letter: Buffer therapy intraventricular haemorrhageJ M Anderson, A D Bain, J K Brown, et al.
American Journal of Medical Genetics|February 1, 1991
Linkage analysis in the fragile X syndrome using multiple distal Xq polymorphic DNA markersI A Glass, L A Pirrit, E M White, et al.
Journal of Medical Genetics|November 1, 1995
Discordant phenylketonuria phenotypes in one family: the relationship between genotype and clinical outcome is a function of multiple effectsL A Tyfield, J Zschocke, A Stephenson, et al.
Archives of Disease in Childhood|November 1, 1986
Dietary copper intake in artificially fed infantsS Salim, J Farquharson, G C Arneil, et al.
American Journal of Human Genetics|February 1, 1997
Sequence variation at the phenylalanine hydroxylase gene in the British IslesL A Tyfield, A Stephenson, F Cockburn, et al.
Tissue & Cell|January 1, 1988
The effects of thermally-induced activity in vivo upon the ultrastructure and Na, K and Cl composition of the epithelial cells of sweat glands from patients with cystic fibrosisS M Wilson, H Y Elder, A M Sutton, et al.
Lancet (London, England)|April 19, 1986
Determination of red-cell mass in assessment and management of anaemia in babies needing blood transfusionH M Phillips, B M Holland, A Abdel-Moiz, et al.
Archives of Disease in Childhood|March 1, 1977
Clinical and biochemical assessment of a modified evaporated milk for infant feedingN R Belton, F Cockburn, J O Forfar, et al.
American Journal of Human Genetics|May 1, 1989
Haplotype distribution of the human phenylalanine hydroxylase locus in Scotland and SwitzerlandS E Sullivan, S D Moore, J M Connor, et al.
Pageof 14

Showing results (121-130 of 134) with videos related to

Sort By:
Pageof 14
Lancet (London, England)|January 17, 1976
Hyaline-membrane disease, alkaline buffer treatment, and cerebral intraventricular halphaemorrhageJ M Anderson, A D Bain, J K Brown, et al.
Lancet (London, England)|February 21, 1976
Letter: Buffer therapy intraventricular haemorrhageJ M Anderson, A D Bain, J K Brown, et al.
American Journal of Medical Genetics|February 1, 1991
Linkage analysis in the fragile X syndrome using multiple distal Xq polymorphic DNA markersI A Glass, L A Pirrit, E M White, et al.
Journal of Medical Genetics|November 1, 1995
Discordant phenylketonuria phenotypes in one family: the relationship between genotype and clinical outcome is a function of multiple effectsL A Tyfield, J Zschocke, A Stephenson, et al.
Archives of Disease in Childhood|November 1, 1986
Dietary copper intake in artificially fed infantsS Salim, J Farquharson, G C Arneil, et al.
American Journal of Human Genetics|February 1, 1997
Sequence variation at the phenylalanine hydroxylase gene in the British IslesL A Tyfield, A Stephenson, F Cockburn, et al.
Tissue & Cell|January 1, 1988
The effects of thermally-induced activity in vivo upon the ultrastructure and Na, K and Cl composition of the epithelial cells of sweat glands from patients with cystic fibrosisS M Wilson, H Y Elder, A M Sutton, et al.
Lancet (London, England)|April 19, 1986
Determination of red-cell mass in assessment and management of anaemia in babies needing blood transfusionH M Phillips, B M Holland, A Abdel-Moiz, et al.
Archives of Disease in Childhood|March 1, 1977
Clinical and biochemical assessment of a modified evaporated milk for infant feedingN R Belton, F Cockburn, J O Forfar, et al.
American Journal of Human Genetics|May 1, 1989
Haplotype distribution of the human phenylalanine hydroxylase locus in Scotland and SwitzerlandS E Sullivan, S D Moore, J M Connor, et al.
Pageof 14