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A Vandenberghe

Showing results (81-90 of 126) with videos related to

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Journal of Neurology, Neurosurgery, and Psychiatry|February 13, 2001
Mild recurrent neuropathy in CMT1B with a novel nonsense mutation in the extracellular domain of the MPZ geneA Lagueny, P Latour, A Vital, et al.
Clinical Chemistry|April 28, 2001
Polymorphic short tandem repeats for diagnosis of the Charcot-Marie-Tooth 1A duplicationP Latour, L Boutrand, N Levy, et al.
Clinical Genetics|December 1, 1995
Charcot-Marie-Tooth type 1B neuropathy: third mutation of serine 63 codon in the major peripheral myelin glycoprotein PO geneF Blanquet-Grossard, D Pham-Dinh, A Dautigny, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1995
Molecular characterization of Charcot-Marie-Tooth patients in 15 pedigrees from FranceG Lucotte, S Berriche, C Bathelier, et al.
Human Genetics|January 1, 1988
The Duffy blood group is linked to the alpha-spectrin locus in a large pedigree with autosomal dominant inheritance of Charcot-Marie-Tooth disease type 1P Raeymaekers, C Van Broeckhoven, H Backhovens, et al.
Human Molecular Genetics|November 5, 1999
Homologous DNA exchanges in humans can be explained by the yeast double-strand break repair model: a study of 17p11.2 rearrangements associated with CMT1A and HNPPJ Lopes, S Tardieu, K Silander, et al.
Biochimica Et Biophysica Acta|February 19, 1998
The antibiotic ceftazidime is a singlet oxygen quencher as demonstrated by ultra-weak chemiluminescence and by inhibition of AAP consumptionG Deby-Dupont, C Deby, A Mouithys-Mickalad, et al.
Somatic Cell and Molecular Genetics|May 1, 1990
Physical mapping of chromosome 21 DNA markers in Alzheimer's disease region using somatic cell hybridsG Van Camp, W Van Hul, H Backhovens, et al.
Archives Internationales De Physiologie Et De Biochimie|October 1, 1974
Proceedings: Information content of an RNA genomeW Fiers, R Contreras, G Haegeman, et al.
Journal of the Neurological Sciences|December 1, 1988
Absence of linkage with the Duffy blood group in a family with Charcot-Marie-Tooth neuropathyP Raeymaekers, P De Jonghe, L Swerts, et al.
Pageof 13

Showing results (81-90 of 126) with videos related to

Sort By:
Pageof 13
Journal of Neurology, Neurosurgery, and Psychiatry|February 13, 2001
Mild recurrent neuropathy in CMT1B with a novel nonsense mutation in the extracellular domain of the MPZ geneA Lagueny, P Latour, A Vital, et al.
Clinical Chemistry|April 28, 2001
Polymorphic short tandem repeats for diagnosis of the Charcot-Marie-Tooth 1A duplicationP Latour, L Boutrand, N Levy, et al.
Clinical Genetics|December 1, 1995
Charcot-Marie-Tooth type 1B neuropathy: third mutation of serine 63 codon in the major peripheral myelin glycoprotein PO geneF Blanquet-Grossard, D Pham-Dinh, A Dautigny, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1995
Molecular characterization of Charcot-Marie-Tooth patients in 15 pedigrees from FranceG Lucotte, S Berriche, C Bathelier, et al.
Human Genetics|January 1, 1988
The Duffy blood group is linked to the alpha-spectrin locus in a large pedigree with autosomal dominant inheritance of Charcot-Marie-Tooth disease type 1P Raeymaekers, C Van Broeckhoven, H Backhovens, et al.
Human Molecular Genetics|November 5, 1999
Homologous DNA exchanges in humans can be explained by the yeast double-strand break repair model: a study of 17p11.2 rearrangements associated with CMT1A and HNPPJ Lopes, S Tardieu, K Silander, et al.
Biochimica Et Biophysica Acta|February 19, 1998
The antibiotic ceftazidime is a singlet oxygen quencher as demonstrated by ultra-weak chemiluminescence and by inhibition of AAP consumptionG Deby-Dupont, C Deby, A Mouithys-Mickalad, et al.
Somatic Cell and Molecular Genetics|May 1, 1990
Physical mapping of chromosome 21 DNA markers in Alzheimer's disease region using somatic cell hybridsG Van Camp, W Van Hul, H Backhovens, et al.
Archives Internationales De Physiologie Et De Biochimie|October 1, 1974
Proceedings: Information content of an RNA genomeW Fiers, R Contreras, G Haegeman, et al.
Journal of the Neurological Sciences|December 1, 1988
Absence of linkage with the Duffy blood group in a family with Charcot-Marie-Tooth neuropathyP Raeymaekers, P De Jonghe, L Swerts, et al.
Pageof 13