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Physiological Research|February 15, 2007
Ursodesoxycholic acid and heme-arginate are unable to improve hematopoiesis and liver injury in an erythropoietic protoporphyria mouse modelM Abitbol, H Puy, J-M Sabaté, et al.Ophtalmologie : Organe De La Societe Francaise D'Ophtalmologie|January 1, 1990
[In situ hybridization on tissue section: a new method for studying the amacrine cells of the retina and the centers of the visual system]M Abitbol, S Dumas, J F Julien, et al.Obstetrics and Gynecology|November 1, 1976
Production of experimental toxemia in the pregnant dogM M Abitbol, C L Pirani, W B Ober, et al.Journal of Neurology, Neurosurgery, and Psychiatry|April 1, 1997
Spinal and cutaneous schwannomatosis is a variant form of type 2 neurofibromatosis: a clinical and molecular studyD G Evans, S Mason, S M Huson, et al.Human Genetics|March 1, 1992
CYP21/C4 gene organisation in Italian 21-hydroxylase deficiency familiesP J Sinnott, C Livieri, M Sampietro, et al.Heart Rhythm|January 28, 2021
Right ventricular insertion promotes reinitiation of ventricular fibrillation in defibrillation failureKenichi Iijima, Hanyu Zhang, Matthew T Strachan, et al.Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|November 6, 1975
DNA-RNA hybridizationJ O Bishop, J S Beckmann, M S Campo, et al.Human Genetics|October 1, 1990
Molecular analysis of the human MHC class I region in hereditary haemochromatosis. A study by pulsed-field gel electrophoresisD K Lord, I Dunham, R D Campbell, et al.Journal of Medical Genetics|June 1, 1995
Diagnostic issues in a family with late onset type 2 neurofibromatosisD G Evans, D Bourn, A Wallace, et al.The EMBO Journal|May 1, 1989
Pulsed field gel electrophoresis identifies a high degree of variability in the number of tandem 21-hydroxylase and complement C4 gene repeats in 21-hydroxylase deficiency haplotypesS Collier, P J Sinnott, P A Dyer, et al.Pageof 96