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Journal of Medical Genetics|December 1, 1991
Selection in blood cells from female carriers of the fragile X syndrome: inverse correlation between age and proportion of active X chromosomes carrying the full mutationF Rousseau, D Heitz, I Oberlé, et al.American Journal of Medical Genetics|April 1, 1992
On some technical aspects of direct DNA diagnosis of the fragile X syndromeF Rousseau, D Heitz, V Biancalana, et al.Current Opinion in Genetics & Development|June 1, 1992
Molecular genetics of the fragile-X syndrome: a novel type of unstable mutationJ L Mandel, D HeitzScience (New York, N.Y.)|May 24, 1991
Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndromeI Oberlé, F Rousseau, D Heitz, et al.Human Genetics|February 1, 1990
New informative polymorphism at the DXS304 locus, a close distal marker for the fragile X locusF Rousseau, A Vincent, I Oberlé, et al.American Journal of Human Genetics|January 1, 1991
Four chromosomal breakpoints and four new probes mark out a 10-cM region encompassing the fragile-X locus (FRAXA)F Rousseau, A Vincent, S Rivella, et al.Journal of Medical Genetics|November 1, 1992
Inheritance of the fragile X syndrome: size of the fragile X premutation is a major determinant of the transition to full mutationD Heitz, D Devys, G Imbert, et al.Nature|February 14, 1991
Abnormal pattern detected in fragile-X patients by pulsed-field gel electrophoresisA Vincent, D Heitz, C Petit, et al.American Journal of Medical Genetics|April 1, 1992
Analysis of full fragile X mutations in fetal tissues and monozygotic twins indicate that abnormal methylation and somatic heterogeneity are established early in developmentD Devys, V Biancalana, F Rousseau, et al.American Journal of Medical Genetics|July 15, 1992
A reinvestigation of thirty three fragile(X) families using probe StB12.3J Macpherson, J Harvey, G Curtis, et al.Pageof 66