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J L Mandel

Showing results (211-220 of 257) with videos related to

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Human Genetics|July 1, 1992
A 530kb YAC contig tightly linked to the Friedreich ataxia locus contains five CpG clusters and a new highly polymorphic microsatelliteR Fujita, G Sirugo, F Duclos, 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.
American Journal of Human Genetics|July 1, 1995
Genetic linkage heterogeneity in myotubular myopathyF Samson, L Mesnard, M Heimburger, et al.
Clinical Genetics|February 26, 2013
Clinical and genetic characterization of Bardet-Biedl syndrome in Tunisia: defining a strategy for molecular diagnosisO M'hamdi, C Redin, C Stoetzel, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
ALDP expression in fibroblasts of patients with X-linked adrenoleukodystrophyS Kemp, P A Mooyer, P A Bolhuis, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 28, 1995
Retroviral-mediated gene transfer corrects very-long-chain fatty acid metabolism in adrenoleukodystrophy fibroblastsN Cartier, J Lopez, P Moullier, et al.
Human Genetics|January 1, 1985
Segregation analysis of a marker localised Xp21.2-Xp21.3 in Duchenne and Becker muscular dystrophy familiesH Dorkins, C Junien, J L Mandel, et al.
American Journal of Human Genetics|December 1, 1992
Study of large inbred Friedreich ataxia families reveals a recombination between D9S15 and the disease locusS Belal, K Panayides, G Sirugo, et al.
Human Genetics|March 1, 1988
Multilocus analysis of the fragile X syndromeW T Brown, A Gross, C Chan, et al.
Journal of Medical Genetics|December 1, 1994
X linked myotubular myopathy (MTM1) maps between DXS304 and DXS305, closely linked to the DXS455 VNTR and a new, highly informative microsatellite marker (DXS1684)N Dahl, F Samson, N S Thomas, et al.
Pageof 26

Showing results (211-220 of 257) with videos related to

Sort By:
Pageof 26
Human Genetics|July 1, 1992
A 530kb YAC contig tightly linked to the Friedreich ataxia locus contains five CpG clusters and a new highly polymorphic microsatelliteR Fujita, G Sirugo, F Duclos, 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.
American Journal of Human Genetics|July 1, 1995
Genetic linkage heterogeneity in myotubular myopathyF Samson, L Mesnard, M Heimburger, et al.
Clinical Genetics|February 26, 2013
Clinical and genetic characterization of Bardet-Biedl syndrome in Tunisia: defining a strategy for molecular diagnosisO M'hamdi, C Redin, C Stoetzel, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
ALDP expression in fibroblasts of patients with X-linked adrenoleukodystrophyS Kemp, P A Mooyer, P A Bolhuis, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 28, 1995
Retroviral-mediated gene transfer corrects very-long-chain fatty acid metabolism in adrenoleukodystrophy fibroblastsN Cartier, J Lopez, P Moullier, et al.
Human Genetics|January 1, 1985
Segregation analysis of a marker localised Xp21.2-Xp21.3 in Duchenne and Becker muscular dystrophy familiesH Dorkins, C Junien, J L Mandel, et al.
American Journal of Human Genetics|December 1, 1992
Study of large inbred Friedreich ataxia families reveals a recombination between D9S15 and the disease locusS Belal, K Panayides, G Sirugo, et al.
Human Genetics|March 1, 1988
Multilocus analysis of the fragile X syndromeW T Brown, A Gross, C Chan, et al.
Journal of Medical Genetics|December 1, 1994
X linked myotubular myopathy (MTM1) maps between DXS304 and DXS305, closely linked to the DXS455 VNTR and a new, highly informative microsatellite marker (DXS1684)N Dahl, F Samson, N S Thomas, et al.
Pageof 26