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The Journal of Otolaryngology|April 1, 1979
[Sialoscintimetry in disorders of the facial nerve]J G Marsan, G Forget, A LevasseurAdvances in Skin & Wound Care|August 21, 2023
The 2022 Update on Pressure Injuries: A Review of the LiteratureDan Berlowitz, Julia G Forget, Kelley SaindonHemoglobin|January 1, 1981
Globin chain electrophoresis for prenatal diagnosis of beta thalassemiaB P Alter, E Coupal, B G ForgetRegenerative Medicine|September 19, 2009
Induced pluripotent stem cells in regenerative medicine: an argument for continued research on human embryonic stem cellsHan Lee, Jung Park, Bernard G Forget, et al.Transactions of the American Clinical and Climatological Association|July 6, 2000
Familial polycythemia due to truncations of the erythropoietin receptorB G Forget, B A Degan, M O ArcasoyMajor Problems in Internal Medicine|January 1, 1977
HemoglobinopathiesH F Bunn, B G Forget, H M RanneyBritish Journal of Haematology|December 1, 1993
Analysis of a PstI polymorphism of the human erythrocyte band 3 gene (EPB3)P B Jenkins, P G Gallagher, B G ForgetExperimental Hematology|January 29, 1999
A human erythropoietin receptor gene mutant causing familial erythrocytosis is associated with deregulation of the rates of Jak2 and Stat5 inactivationM O Arcasoy, K W Harris, B G ForgetBlood|November 1, 1986
A novel basis for delta beta-thalassemia in a Chinese familyG F Atweh, D E Zhu, B G ForgetAmerican Journal of Human Genetics|March 1, 1988
Analyses of linked beta-globin genes suggest that nondeletion forms of hereditary persistence of fetal hemoglobin are bona fide switching mutantsJ E Metherall, F P Gillespie, B G ForgetPageof 18