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A Fryer

Showing results (111-120 of 378) with videos related to

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Medical Science Monitor : International Medical Journal of Experimental and Clinical Research|April 28, 2009
Fibrillin 1 gene with R2726W mutation is absent in patients with primary protrusio acetabuli and developmental dysplasia of the hipSubhajit Ghosh, Anthony A Fryer, Paul R Hoban, et al.
Gut|June 1, 1990
Porphyria cutanea tarda and haemochromatosis: a family studyD G Seymour, G H Elder, A Fryer, et al.
Health Expectations : an International Journal of Public Participation in Health Care and Health Policy|May 16, 2026
Frameworks to Evaluate the Quality of Public Involvement in Health and Social Care Research: A Scoping ReviewRose Hutton, Alice Moult, Dereth Baker, et al.
Methods in Molecular Biology (Clifton, N.J.)|July 19, 2020
Mapping Transcriptome-Wide and Genome-Wide RNA-DNA Contacts with Chromatin-Associated RNA Sequencing (ChAR-seq)Charles Limouse, David Jukam, Owen K Smith, et al.
Clinical and Experimental Allergy : Journal of the British Society for Allergy and Clinical Immunology|July 9, 2002
An association study between the Clara cell secretory protein CC16 A38G polymorphism and asthma phenotypesA H Mansur, A A Fryer, M Hepple, et al.
Journal of the Royal Society of Medicine|May 18, 1999
Basal cell carcinomaJ T Lear, I Harvey, D de Berker, et al.
BMJ (Clinical Research Ed.)|January 20, 2018
Management of incidental adrenal tumoursFahmy W F Hanna, Basil G Issa, Julius Sim, et al.
Arthritis and Rheumatism|October 1, 1996
Association of homozygosity for glutathione-S-transferase GSTM1 null alleles with the Ro+/La- autoantibody profile in patients with systemic lupus erythematosusW Ollier, E Davies, N Snowden, et al.
Journal of Medical Genetics|March 1, 1992
Prenatal diagnosis and presymptomatic detection of neurofibromatosis type 1M Upadhyaya, A Fryer, J MacMillan, et al.
The Journal of Laboratory and Clinical Medicine|November 1, 1990
Lipid peroxidation and expression of copper-zinc and manganese superoxide dismutase in lungs of premature infants with hyaline membrane disease and bronchopulmonary dysplasiaR C Strange, W Cotton, A A Fryer, et al.
Pageof 38

Showing results (111-120 of 378) with videos related to

Sort By:
Pageof 38
Medical Science Monitor : International Medical Journal of Experimental and Clinical Research|April 28, 2009
Fibrillin 1 gene with R2726W mutation is absent in patients with primary protrusio acetabuli and developmental dysplasia of the hipSubhajit Ghosh, Anthony A Fryer, Paul R Hoban, et al.
Gut|June 1, 1990
Porphyria cutanea tarda and haemochromatosis: a family studyD G Seymour, G H Elder, A Fryer, et al.
Health Expectations : an International Journal of Public Participation in Health Care and Health Policy|May 16, 2026
Frameworks to Evaluate the Quality of Public Involvement in Health and Social Care Research: A Scoping ReviewRose Hutton, Alice Moult, Dereth Baker, et al.
Methods in Molecular Biology (Clifton, N.J.)|July 19, 2020
Mapping Transcriptome-Wide and Genome-Wide RNA-DNA Contacts with Chromatin-Associated RNA Sequencing (ChAR-seq)Charles Limouse, David Jukam, Owen K Smith, et al.
Clinical and Experimental Allergy : Journal of the British Society for Allergy and Clinical Immunology|July 9, 2002
An association study between the Clara cell secretory protein CC16 A38G polymorphism and asthma phenotypesA H Mansur, A A Fryer, M Hepple, et al.
Journal of the Royal Society of Medicine|May 18, 1999
Basal cell carcinomaJ T Lear, I Harvey, D de Berker, et al.
BMJ (Clinical Research Ed.)|January 20, 2018
Management of incidental adrenal tumoursFahmy W F Hanna, Basil G Issa, Julius Sim, et al.
Arthritis and Rheumatism|October 1, 1996
Association of homozygosity for glutathione-S-transferase GSTM1 null alleles with the Ro+/La- autoantibody profile in patients with systemic lupus erythematosusW Ollier, E Davies, N Snowden, et al.
Journal of Medical Genetics|March 1, 1992
Prenatal diagnosis and presymptomatic detection of neurofibromatosis type 1M Upadhyaya, A Fryer, J MacMillan, et al.
The Journal of Laboratory and Clinical Medicine|November 1, 1990
Lipid peroxidation and expression of copper-zinc and manganese superoxide dismutase in lungs of premature infants with hyaline membrane disease and bronchopulmonary dysplasiaR C Strange, W Cotton, A A Fryer, et al.
Pageof 38