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American Journal of Medical Genetics|May 1, 1988
Improved DNA markers for efficient analysis of fragile X familiesR Heilig, I Oberlé, B Arveiler, et al.Biochimica Et Biophysica Acta|September 19, 1995
Isolation of cDNA clone encoding human homologue of senescence marker protein-30 (SMP30) and its location on the X chromosomeT Fujita, J L Mandel, T Shirasawa, et al.Nature|July 9, 1987
Localization of the region homologous to the Duchenne muscular dystrophy locus on the mouse X chromosomeR Heilig, C Lemaire, J L Mandel, 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.Science (New York, N.Y.)|October 2, 1992
Genome analysis and the human X chromosomeJ L Mandel, A P Monaco, D L Nelson, et al.FEBS Letters|April 1, 1997
Fenofibrate differently alters expression of genes encoding ATP-binding transporter proteins of the peroxisomal membraneS Albet, C Causeret, M Bentejac, et al.Cell|February 1, 1981
The ovalbumin gene family: hormonal control of X and Y gene transcription and mRNA accumulationM LeMeur, N Glanville, J L Mandel, et al.Nature|December 15, 1983
Close linkage of fragile X-mental retardation syndrome to haemophilia B and transmission through a normal maleG Camerino, M G Mattei, J F Mattei, et al.American Journal of Medical Genetics|July 15, 1994
Non-specific X-linked mental retardation: linkage analysis in MRX2 and MRX4 families revisitedL J Hu, S Blumenfeld-Heyberger, A Hanauer, et al.European Journal of Human Genetics : EJHG|January 1, 1993
Striking founder effect for the fragile X syndrome in FinlandC Oudet, H von Koskull, A M Nordström, et al.Pageof 20