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Nature Reviews. Genetics|September 5, 2001
Monogenic causes of X-linked mental retardationJ Chelly, J L MandelCurrent Opinion in Genetics & Development|June 1, 1992
Molecular genetics of the fragile-X syndrome: a novel type of unstable mutationJ L Mandel, D HeitzMolecular and Cellular Biology|December 1, 1993
Gal80 proteins of Kluyveromyces lactis and Saccharomyces cerevisiae are highly conserved but contribute differently to glucose repression of the galactose regulonF T Zenke, W Zachariae, A Lunkes, et al.Journal of Cellular Physiology|December 1, 1978
Isolation of mutant mammalian cells altered in polyamine transportJ L Mandel, W F FlintoffAnnals of Neurology|July 18, 2001
Diagnosis of X-linked myotubular myopathy by detection of myotubularinJ Laporte, W Kress, J L MandelBrain Research Bulletin|November 24, 2001
The Fragile X mental retardation proteinB Bardoni, A Schenck, J L MandelGenomics|May 1, 1989
Toward a physical map of the Xq28 region in man: linking color vision, G6PD, and coagulation factor VIII genes to an X-Y homology regionB Arveiler, A Vincent, J L MandelGenomics|September 1, 1987
Genetic mapping of nine DNA markers in the q11----q22 region of the human X chromosomeB Arveiler, I Oberlé, J L MandelNucleic Acids Research|November 25, 1987
A 230kb cosmid walk in the Duchenne muscular dystrophy gene: detection of a conserved sequence and of a possible deletion prone regionR Heilig, C Lemaire, J L MandelPageof 20