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Cytogenetics and Cell Genetics|January 1, 1993
An irradiation-reduced hybrid panel for fine-structure mapping of the Xq28 region in the human genomeB Peterlin, A Smahi, L Holvoet-Vermaut, et al.Human Genetics|October 1, 1995
Genetic mapping of Xp22.12-p22.31, with a refined localization for spondyloepiphyseal dysplasia (SEDL)S Heuertz, A Smahi, A O Wilkie, et al.La Revue De Medecine Interne|July 5, 2022
[Autoinflammatory diseases associated with RIPK1 mutations: A review of the literature]A S Parentelli, C Picard, G Boursier, et al.Nucleic Acids Research|February 25, 1987
Characterization of the 5'-flanking region for the human fibrinogen beta geneP Huber, J Dalmon, G Courtois, et al.Journal of Virology|August 1, 1994
Characterization of mpl cytoplasmic domain sequences required for myeloproliferative leukemia virus pathogenicityL Bénit, G Courtois, M Charon, et al.Science (New York, N.Y.)|October 30, 1987
Interaction of a liver-specific nuclear factor with the fibrinogen and alpha 1-antitrypsin promotersG Courtois, J G Morgan, L A Campbell, et al.American Journal of Human Genetics|March 26, 1999
A gene for X-linked idiopathic congenital nystagmus (NYS1) maps to chromosome Xp11.4-p11.3A Cabot, J M Rozet, S Gerber, et al.Journal of Virology|May 1, 1995
Constitutive activation of a variant of the env-mpl oncogene product by disulfide-linked homodimerizationG Courtois, L Bénit, Y Mikaeloff, et al.Transfusion Clinique Et Biologique : Journal De La Societe Francaise De Transfusion Sanguine|May 7, 2013
[HSP70, an erythropoiesis regulator that determines the fate of erythroblasts between death and differentiation]O Hermine, J-B Arlet, J-A Ribeil, et al.Biochemical and Biophysical Research Communications|April 30, 1984
Analysis of fibrinogen genes in patients with congenital afibrinogenemiaG Uzan, G Courtois, C Besmond, et al.Pageof 7