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L Mandel

Showing results (251-260 of 451) with videos related to

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Human Genetics|October 1, 1988
Genetic mapping of anhidrotic ectodermal dysplasia: DXS159, a closely linked proximal markerA Hanauer, Y Alembik, B Arveiler, et al.
Bioorganic & Medicinal Chemistry Letters|August 8, 2007
A synthetic entry to pladienolide B and FD-895Alexander L Mandel, Brian D Jones, James J La Clair, 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.
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.
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.
EXS|January 1, 1993
Microsatellites and disease: a new paradigmK Wrogemann, V Biancalana, D Devys, et al.
Pageof 46

Showing results (251-260 of 451) with videos related to

Sort By:
Pageof 46
Human Genetics|October 1, 1988
Genetic mapping of anhidrotic ectodermal dysplasia: DXS159, a closely linked proximal markerA Hanauer, Y Alembik, B Arveiler, et al.
Bioorganic & Medicinal Chemistry Letters|August 8, 2007
A synthetic entry to pladienolide B and FD-895Alexander L Mandel, Brian D Jones, James J La Clair, 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.
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.
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.
EXS|January 1, 1993
Microsatellites and disease: a new paradigmK Wrogemann, V Biancalana, D Devys, et al.
Pageof 46