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Blood|May 30, 1998
A large deletion within the protein 4.1 gene associated with a stable truncated mRNA and an unaltered tissue-specific alternative splicingN D Venezia, P Maillet, L Morlé, et al.Leukemia|November 1, 1992
Expression of the serglycin gene in human leukemic cell linesP Maillet, P M Alliel, M T Mitjavila, et al.FEBS Letters|August 15, 1988
Complete amino acid sequence of a human platelet proteoglycanP M Alliel, J P Périn, P Maillet, et al.Annales De Genetique|January 1, 1996
Molecular genetics of hereditary elliptocytosis and hereditary spherocytosisJ Delaunay, N Alloisio, L Morle, et al.Nephrologie|January 1, 1985
[Retroperitoneal fibrosis and generalized scleroderma]P Cochat, S Colon, M Laville, et al.Annales D'Endocrinologie|January 1, 1977
[Endocrine polyadenomatosis associated with prolactin pituitary adenoma and an intrathyroidal parathyroid adenoma]J Tourniaire, J Trouillas, P Maillet, et al.Blood|August 1, 1996
Hereditary spherocytosis with band 3 deficiency. Association with a nonsense mutation of the band 3 gene (allele Lyon), and aggravation by a low-expression allele occurring in trans (allele Genas)N Alloisio, P Maillet, G Carré, et al.International Journal of Cancer|November 28, 2000
A polymorphism in the ATM gene modulates the penetrance of hereditary non-polyposis colorectal cancerP Maillet, P O Chappuis, G Vaudan, et al.JDR Clinical and Translational Research|April 2, 2019
Factors Influencing Adoption of New Technologies into Dental Practice: A Qualitative StudyD C Matthews, K McNeil, M Brillant, et al.Human Mutation|July 29, 1999
A premature termination codon within an alternative exon affecting only the metabolism of transcripts that retain this exonP Maillet, N Dalla Venezia, F Lorenzo, et al.Pageof 5