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J L Mandel

Showing results (101-110 of 257) with videos related to

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Nature|February 14, 1991
Abnormal pattern detected in fragile-X patients by pulsed-field gel electrophoresisA Vincent, D Heitz, C Petit, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 6, 1996
A close relative of the adrenoleukodystrophy (ALD) gene codes for a peroxisomal protein with a specific expression patternG Lombard-Platet, S Savary, C O Sarde, et al.
American Journal of Human Genetics|May 1, 1990
Germ-line mosaicism simulates genetic heterogeneity in Wiskott-Aldrich syndromeB Arveiler, G de Saint-Basile, A Fischer, et al.
The EMBO Journal|September 5, 2001
The fragile X mental retardation protein binds specifically to its mRNA via a purine quartet motifC Schaeffer, B Bardoni, J L Mandel, et al.
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.
Lancet (London, England)|April 13, 1985
Polymorphic DNA markers in prenatal diagnosis of fragile X syndromeI Oberlé, J L Mandel, J Boué, 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.
Pageof 26

Showing results (101-110 of 257) with videos related to

Sort By:
Pageof 26
Nature|February 14, 1991
Abnormal pattern detected in fragile-X patients by pulsed-field gel electrophoresisA Vincent, D Heitz, C Petit, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 6, 1996
A close relative of the adrenoleukodystrophy (ALD) gene codes for a peroxisomal protein with a specific expression patternG Lombard-Platet, S Savary, C O Sarde, et al.
American Journal of Human Genetics|May 1, 1990
Germ-line mosaicism simulates genetic heterogeneity in Wiskott-Aldrich syndromeB Arveiler, G de Saint-Basile, A Fischer, et al.
The EMBO Journal|September 5, 2001
The fragile X mental retardation protein binds specifically to its mRNA via a purine quartet motifC Schaeffer, B Bardoni, J L Mandel, et al.
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.
Lancet (London, England)|April 13, 1985
Polymorphic DNA markers in prenatal diagnosis of fragile X syndromeI Oberlé, J L Mandel, J Boué, 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.
Pageof 26