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J L Mandel

Showing results (171-180 of 257) with videos related to

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American Journal of Human Genetics|December 1, 1991
Adrenoleukodystrophy: a complex chromosomal rearrangement in the Xq28 red/green-color-pigment gene region indicates two possible gene localizationsR Feil, P Aubourg, J Mosser, et al.
American Journal of Human Genetics|December 5, 1998
Mutation analysis of the RSK2 gene in Coffin-Lowry patients: extensive allelic heterogeneity and a high rate of de novo mutationsS Jacquot, K Merienne, D De Cesare, et al.
Human Genetics|May 1, 1994
Hypomagnesemia with secondary hypocalcemia in a female with balanced X;9 translocation: mapping of the Xp22 chromosome breakpointM Chery, V Biancalana, C Philippe, et al.
Genomics|April 1, 1988
Conservation and reorganization of loci on the mammalian X chromosome: a molecular framework for the identification of homologous subchromosomal regions in man and mouseL C Amar, L Dandolo, A Hanauer, et al.
Neuromuscular Disorders : NMD|October 12, 2001
Normal innervation and differentiation of X-linked myotubular myopathy muscle cells in a nerve-muscle coculture systemO M Dorchies, J Laporte, S Wagner, et al.
American Journal of Human Genetics|April 16, 1998
Ataxia with isolated vitamin E deficiency: heterogeneity of mutations and phenotypic variability in a large number of familiesL Cavalier, K Ouahchi, H J Kayden, et al.
Human Molecular Genetics|October 1, 1994
Identification of a new frameshift mutation (1801delAG) in the ALD geneA Barceló, M Girós, C O Sarde, et al.
Cytogenetics and Cell Genetics|January 1, 1989
Report of the committee on the genetic constitution of the X chromosomeJ L Mandel, H F Willard, R L Nussbaum, et al.
Journal Francais D'Ophtalmologie|March 16, 2005
[Update on Bardet-Biedl syndrome]H Dollfus, A Verloes, D Bonneau, et al.
Genomics|July 1, 1994
Genomic organization of the adrenoleukodystrophy geneC O Sarde, J Mosser, P Kioschis, et al.
Pageof 26

Showing results (171-180 of 257) with videos related to

Sort By:
Pageof 26
American Journal of Human Genetics|December 1, 1991
Adrenoleukodystrophy: a complex chromosomal rearrangement in the Xq28 red/green-color-pigment gene region indicates two possible gene localizationsR Feil, P Aubourg, J Mosser, et al.
American Journal of Human Genetics|December 5, 1998
Mutation analysis of the RSK2 gene in Coffin-Lowry patients: extensive allelic heterogeneity and a high rate of de novo mutationsS Jacquot, K Merienne, D De Cesare, et al.
Human Genetics|May 1, 1994
Hypomagnesemia with secondary hypocalcemia in a female with balanced X;9 translocation: mapping of the Xp22 chromosome breakpointM Chery, V Biancalana, C Philippe, et al.
Genomics|April 1, 1988
Conservation and reorganization of loci on the mammalian X chromosome: a molecular framework for the identification of homologous subchromosomal regions in man and mouseL C Amar, L Dandolo, A Hanauer, et al.
Neuromuscular Disorders : NMD|October 12, 2001
Normal innervation and differentiation of X-linked myotubular myopathy muscle cells in a nerve-muscle coculture systemO M Dorchies, J Laporte, S Wagner, et al.
American Journal of Human Genetics|April 16, 1998
Ataxia with isolated vitamin E deficiency: heterogeneity of mutations and phenotypic variability in a large number of familiesL Cavalier, K Ouahchi, H J Kayden, et al.
Human Molecular Genetics|October 1, 1994
Identification of a new frameshift mutation (1801delAG) in the ALD geneA Barceló, M Girós, C O Sarde, et al.
Cytogenetics and Cell Genetics|January 1, 1989
Report of the committee on the genetic constitution of the X chromosomeJ L Mandel, H F Willard, R L Nussbaum, et al.
Journal Francais D'Ophtalmologie|March 16, 2005
[Update on Bardet-Biedl syndrome]H Dollfus, A Verloes, D Bonneau, et al.
Genomics|July 1, 1994
Genomic organization of the adrenoleukodystrophy geneC O Sarde, J Mosser, P Kioschis, et al.
Pageof 26