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

J M Old

Showing results (81-90 of 99) with videos related to

Pageof 10
Sort By:
British Journal of Haematology|March 1, 1987
Association of thalassaemia intermedia with a beta-globin gene haplotypeS L Thein, J S Wainscoat, M Sampietro, et al.
Lancet (London, England)|August 11, 1979
Negro alpha-thalassaemia is caused by deletion of a single alpha-globin geneD R Higgs, L Pressley, J M Old, et al.
Journal of Medical Genetics|February 1, 1986
Meiotic recombination between two polymorphic restriction sites within the beta globin gene clusterJ M Old, C Heath, A Fitches, et al.
Annals of the New York Academy of Sciences|January 1, 1985
First trimester diagnosis of the hemoglobin disordersJ M Old, D J Weatherall, R H Ward, et al.
Journal of Medical Genetics|January 1, 1988
Evidence linking familial thrombosis with a defective antithrombin III gene in two British kindredsS H Sacks, J M Old, S T Reeders, et al.
Annals of the New York Academy of Sciences|January 1, 1985
Genetic and molecular analysis of mild forms of homozygous beta-thalassemiaD J Weatherall, J S Wainscoat, S L Thein, et al.
British Journal of Haematology|August 1, 1992
The beta-thalassaemia mutations in the population of CyprusE Baysal, K Indrak, G Bozkurt, et al.
Hemoglobin|March 19, 1999
The association of Hb Khartoum [beta124(H2)Pro-->Arg] with gamma+-thalassemia is responsible for hemolytic disease in the newborn of a Sudanese familyR A Bayoumi, A Dawodu, M M Qureshi, et al.
The British Journal of Surgery|October 1, 1978
The combination of proximal gastric vagotomy with a rotational posterior gastropexy for duodenal ulcerD M Hancock, M Y Sankar, J M Old, et al.
Human Genetics|January 1, 1985
Segregation analysis of a marker localised Xp21.2-Xp21.3 in Duchenne and Becker muscular dystrophy familiesH Dorkins, C Junien, J L Mandel, et al.
Pageof 10

Showing results (81-90 of 99) with videos related to

Sort By:
Pageof 10
British Journal of Haematology|March 1, 1987
Association of thalassaemia intermedia with a beta-globin gene haplotypeS L Thein, J S Wainscoat, M Sampietro, et al.
Lancet (London, England)|August 11, 1979
Negro alpha-thalassaemia is caused by deletion of a single alpha-globin geneD R Higgs, L Pressley, J M Old, et al.
Journal of Medical Genetics|February 1, 1986
Meiotic recombination between two polymorphic restriction sites within the beta globin gene clusterJ M Old, C Heath, A Fitches, et al.
Annals of the New York Academy of Sciences|January 1, 1985
First trimester diagnosis of the hemoglobin disordersJ M Old, D J Weatherall, R H Ward, et al.
Journal of Medical Genetics|January 1, 1988
Evidence linking familial thrombosis with a defective antithrombin III gene in two British kindredsS H Sacks, J M Old, S T Reeders, et al.
Annals of the New York Academy of Sciences|January 1, 1985
Genetic and molecular analysis of mild forms of homozygous beta-thalassemiaD J Weatherall, J S Wainscoat, S L Thein, et al.
British Journal of Haematology|August 1, 1992
The beta-thalassaemia mutations in the population of CyprusE Baysal, K Indrak, G Bozkurt, et al.
Hemoglobin|March 19, 1999
The association of Hb Khartoum [beta124(H2)Pro-->Arg] with gamma+-thalassemia is responsible for hemolytic disease in the newborn of a Sudanese familyR A Bayoumi, A Dawodu, M M Qureshi, et al.
The British Journal of Surgery|October 1, 1978
The combination of proximal gastric vagotomy with a rotational posterior gastropexy for duodenal ulcerD M Hancock, M Y Sankar, J M Old, et al.
Human Genetics|January 1, 1985
Segregation analysis of a marker localised Xp21.2-Xp21.3 in Duchenne and Becker muscular dystrophy familiesH Dorkins, C Junien, J L Mandel, et al.
Pageof 10