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Human Molecular Genetics|May 1, 1995
A heterogeneous set of FMR1 proteins is widely distributed in mouse tissues and is modulated in cell cultureE W Khandjian, A Fortin, A Thibodeau, et al.American Journal of Human Genetics|August 1, 1994
A multicenter study on genotype-phenotype correlations in the fragile X syndrome, using direct diagnosis with probe StB12.3: the first 2,253 casesF Rousseau, D Heitz, J Tarleton, et al.La Revue Du Praticien|January 15, 1997
[Genetic diseases and unstable expansions of trinucleotide repeats]J L MandelAmerican Journal of Medical Genetics|July 15, 1994
Towards identification of X-linked mental retardation genes: a proposalJ L MandelScience (New York, N.Y.)|March 8, 1991
Isolation of sequences that span the fragile X and identification of a fragile X-related CpG islandD Heitz, F Rousseau, D Devys, et al.American Journal of Medical Genetics|February 1, 1991
New polymorphism and a new chromosome breakpoint establish the physical and genetic mapping of DXS369 in the DXS98-FRAXA intervalI Oberlé, A Vincent, N Abbadi, et al.La Revue De Medecine Interne|January 23, 2004
[Antibiotic-associated diarrhea in the elderly]G Kaltenbach, D HeitzHuman Molecular Genetics|November 18, 1998
Novel isoforms of the fragile X related protein FXR1P are expressed during myogenesisE W Khandjian, B Bardoni, F Corbin, et al.European Journal of Clinical Investigation|January 1, 1994
The fragile X syndrome: implications of molecular genetics for the clinical syndromeF RousseauHuman Molecular Genetics|August 13, 1998
A cellular model that recapitulates major pathogenic steps of Huntington's diseaseA Lunkes, J L MandelPageof 66