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Pediatric Research|October 1, 1984
Molecular defect of spectrin in the family of a child with congenital hemolytic poikilocytic anemiaD Dhermy, M C Lecomte, M Garbarz, et al.The Journal of Clinical Investigation|October 1, 1982
Spectrin beta-chain variant associated with hereditary elliptocytosisD Dhermy, M C Lecomte, M Garbarz, et al.Human Genetics|December 1, 1987
Hereditary pyropoikilocytosis and elliptocytosis in a Caucasian family. Transmission of the same molecular defect in spectrin through three generations with different clinical expressionM C Lecomte, D Dhermy, M Garbarz, et al.Journal of Cancer|November 30, 2012
Primary anorectal melanoma: an updateP Carcoforo, M T Raiji, G M Palini, et al.American Journal of Hematology|July 1, 1988
Hemoglobin J Guantanamo [alpha 2 beta 2 128 (H6) Ala----Asp] in association with hemoglobin C and alpha-thalassemia in a family from BeninH Wajcman, V Baudin-Chich, J Kister, et al.British Journal of Haematology|July 1, 1990
A haemolytic syndrome associated with the complete absence of red cell membrane protein 4.2 in two Tunisian siblingsA Ghanem, B Pothier, J Marechal, et al.Water Research|January 6, 2007
Retention of inorganic arsenic by coryneform mutant strainsJ C Feo, E Ordoñez, M Letek, et al.The Analyst|May 29, 2009
A candidate serum biomarker for bladder pain syndrome/interstitial cystitisDaniel E Rubio-Diaz, Megan E Pozza, Jordan Dimitrakov, et al.Journal of the American College of Surgeons|April 17, 1998
Laparoscopic repair of paraesophageal hiatal herniasW A Gantert, M G Patti, M Arcerito, et al.Pageof 18