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P Burlet

Showing results (1-10 of 32) with videos related to

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Archives Des Maladies Professionnelles De Medecine Du Travail Et De Securite Sociale|April 1, 1972
[Dermatoses caused by melamine]R Soubrier, P Burlet
American Journal of Human Genetics|May 1, 1992
Proximal spinal muscular atrophy (SMA) types II and III in the same sibship are not caused by different alleles at the SMA locus on 5qB Müller, J Melki, P Burlet, et al.
Lancet (London, England)|December 23, 1995
SMN gene deletions in adult-onset spinal muscular atrophyO Clermont, P Burlet, S Lefebvre, et al.
Human Molecular Genetics|August 1, 1993
Trinucleotide repeat polymorphism at the D5S556 locusP Burlet, S Abdelhak, F Pascal, et al.
Journal of Medical Genetics|April 1, 1996
Large scale deletions of the 5q13 region are specific to Werdnig-Hoffmann diseaseP Burlet, L Bürglen, O Clermont, et al.
Nucleic Acids Research|September 25, 1990
A PstI polymorphism at the D5S39 locusS Abdelhak, J Melki, M F Bachelot, et al.
Cytogenetics and Cell Genetics|January 1, 1991
In situ hybridization of two markers closely flanking the spinal muscular atrophy gene to 5q12----q13.3M G Mattei, J Melki, M F Bachelot, et al.
Genomics|March 15, 1996
Structure and organization of the human survival motor neurone (SMN) geneL Bürglen, S Lefebvre, O Clermont, et al.
Nature Genetics|July 1, 1997
Correlation between severity and SMN protein level in spinal muscular atrophyS Lefebvre, P Burlet, Q Liu, et al.
Human Molecular Genetics|April 10, 1999
The RNA-binding properties of SMN: deletion analysis of the zebrafish orthologue defines domains conserved in evolutionS Bertrandy, P Burlet, O Clermont, et al.
Pageof 4

Showing results (1-10 of 32) with videos related to

Sort By:
Pageof 4
Archives Des Maladies Professionnelles De Medecine Du Travail Et De Securite Sociale|April 1, 1972
[Dermatoses caused by melamine]R Soubrier, P Burlet
American Journal of Human Genetics|May 1, 1992
Proximal spinal muscular atrophy (SMA) types II and III in the same sibship are not caused by different alleles at the SMA locus on 5qB Müller, J Melki, P Burlet, et al.
Lancet (London, England)|December 23, 1995
SMN gene deletions in adult-onset spinal muscular atrophyO Clermont, P Burlet, S Lefebvre, et al.
Human Molecular Genetics|August 1, 1993
Trinucleotide repeat polymorphism at the D5S556 locusP Burlet, S Abdelhak, F Pascal, et al.
Journal of Medical Genetics|April 1, 1996
Large scale deletions of the 5q13 region are specific to Werdnig-Hoffmann diseaseP Burlet, L Bürglen, O Clermont, et al.
Nucleic Acids Research|September 25, 1990
A PstI polymorphism at the D5S39 locusS Abdelhak, J Melki, M F Bachelot, et al.
Cytogenetics and Cell Genetics|January 1, 1991
In situ hybridization of two markers closely flanking the spinal muscular atrophy gene to 5q12----q13.3M G Mattei, J Melki, M F Bachelot, et al.
Genomics|March 15, 1996
Structure and organization of the human survival motor neurone (SMN) geneL Bürglen, S Lefebvre, O Clermont, et al.
Nature Genetics|July 1, 1997
Correlation between severity and SMN protein level in spinal muscular atrophyS Lefebvre, P Burlet, Q Liu, et al.
Human Molecular Genetics|April 10, 1999
The RNA-binding properties of SMN: deletion analysis of the zebrafish orthologue defines domains conserved in evolutionS Bertrandy, P Burlet, O Clermont, et al.
Pageof 4