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P Burlet

Showing results (21-30 of 32) with videos related to

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Science (New York, N.Y.)|June 3, 1994
De novo and inherited deletions of the 5q13 region in spinal muscular atrophiesJ Melki, S Lefebvre, L Burglen, et al.
Molecular Human Reproduction|August 10, 2006
Multiple displacement amplification improves PGD for fragile X syndromeP Burlet, N Frydman, N Gigarel, et al.
Genomics|September 1, 1993
Machado-Joseph disease is genetically different from Holguin dominant ataxia (SCA2)I Silveira, A Manaia, J Melki, et al.
American Journal of Human Genetics|April 1, 1994
Use of genetic and physical mapping to locate the spinal muscular atrophy locus between two new highly polymorphic DNA markersO Clermont, P Burlet, L Burglen, et al.
Nature|April 19, 1990
Gene for chronic proximal spinal muscular atrophies maps to chromosome 5qJ Melki, S Abdelhak, P Sheth, et al.
The Journal of Clinical Investigation|September 1, 1996
Survival motor neuron gene deletion in the arthrogryposis multiplex congenita-spinal muscular atrophy associationL Bürglen, J Amiel, L Viollet, et al.
Genomics|February 15, 1997
cDNA isolation, expression, and chromosomal localization of the mouse survival motor neuron gene (Smn)L Viollet, S Bertrandy, A L Bueno Brunialti, et al.
American Journal of Human Genetics|April 1, 1991
Linkage analysis in spinal muscular atrophy, by six closely flanking markers on chromosome 5P Sheth, S Abdelhak, M F Bachelot, et al.
Human Molecular Genetics|November 13, 1998
The distribution of SMN protein complex in human fetal tissues and its alteration in spinal muscular atrophyP Burlet, C Huber, S Bertrandy, et al.
Journal of Medical Genetics|September 13, 2005
Analysis of mtDNA variant segregation during early human embryonic development: a tool for successful NARP preimplantation diagnosisJ Steffann, N Frydman, N Gigarel, et al.
Pageof 4

Showing results (21-30 of 32) with videos related to

Sort By:
Pageof 4
Science (New York, N.Y.)|June 3, 1994
De novo and inherited deletions of the 5q13 region in spinal muscular atrophiesJ Melki, S Lefebvre, L Burglen, et al.
Molecular Human Reproduction|August 10, 2006
Multiple displacement amplification improves PGD for fragile X syndromeP Burlet, N Frydman, N Gigarel, et al.
Genomics|September 1, 1993
Machado-Joseph disease is genetically different from Holguin dominant ataxia (SCA2)I Silveira, A Manaia, J Melki, et al.
American Journal of Human Genetics|April 1, 1994
Use of genetic and physical mapping to locate the spinal muscular atrophy locus between two new highly polymorphic DNA markersO Clermont, P Burlet, L Burglen, et al.
Nature|April 19, 1990
Gene for chronic proximal spinal muscular atrophies maps to chromosome 5qJ Melki, S Abdelhak, P Sheth, et al.
The Journal of Clinical Investigation|September 1, 1996
Survival motor neuron gene deletion in the arthrogryposis multiplex congenita-spinal muscular atrophy associationL Bürglen, J Amiel, L Viollet, et al.
Genomics|February 15, 1997
cDNA isolation, expression, and chromosomal localization of the mouse survival motor neuron gene (Smn)L Viollet, S Bertrandy, A L Bueno Brunialti, et al.
American Journal of Human Genetics|April 1, 1991
Linkage analysis in spinal muscular atrophy, by six closely flanking markers on chromosome 5P Sheth, S Abdelhak, M F Bachelot, et al.
Human Molecular Genetics|November 13, 1998
The distribution of SMN protein complex in human fetal tissues and its alteration in spinal muscular atrophyP Burlet, C Huber, S Bertrandy, et al.
Journal of Medical Genetics|September 13, 2005
Analysis of mtDNA variant segregation during early human embryonic development: a tool for successful NARP preimplantation diagnosisJ Steffann, N Frydman, N Gigarel, et al.
Pageof 4