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J Chelly

Showing results (41-50 of 157) with videos related to

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Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|June 23, 2009
[Phenotypic heterogeneity of Duchenne myopathy and prognosis criteria]I Desguerre, M Mayer, C Christov, et al.
Revue Neurologique|January 28, 2020
Benign hereditary chorea: From benign to seriousA Lamiral, S El Chehadeh, J Chelly, et al.
Biochemical and Biophysical Research Communications|July 31, 1991
Illegitimate (or ectopic) transcription proceeds through the usual promotersJ Chelly, J P Hugnot, J P Concordet, et al.
Cell|June 17, 1994
Isolation of the gene for McLeod syndrome that encodes a novel membrane transport proteinM Ho, J Chelly, N Carter, et al.
Annales De L'Anesthesiologie Francaise|January 1, 1979
[Anesthesia for aorto-coronary bypass]B Fontaine, E Bertrandias, D Tournay, et al.
Genomics|April 10, 1995
Characterization of the exon structure of the Menkes disease gene using vectorette PCRZ Tümer, B Vural, T Tønnesen, et al.
Revue Neurologique|January 18, 2021
Paroxysmal dyskinesia: When a PRRT2 variant hides a curable causeV Schneider, M Ferrari-Henquinet, A O Diallo, et al.
European Journal of Biochemistry|February 14, 1990
Quantitative estimation of minor mRNAs by cDNA-polymerase chain reaction. Application to dystrophin mRNA in cultured myogenic and brain cellsJ Chelly, D Montarras, C Pinset, et al.
Human Genetics|December 1, 1987
Familial deletion of Xp21.2 with glycerol kinase deficiency and congenital adrenal hypoplasiaF Marlhens, J Chelly, J C Kaplan, et al.
Journal of Medical Genetics|January 5, 2002
Evidence of somatic mosaicism for a MECP2 mutation in females with Rett syndrome: diagnostic implicationsV Bourdon, C Philippe, T Bienvenu, et al.
Pageof 16

Showing results (41-50 of 157) with videos related to

Sort By:
Pageof 16
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|June 23, 2009
[Phenotypic heterogeneity of Duchenne myopathy and prognosis criteria]I Desguerre, M Mayer, C Christov, et al.
Revue Neurologique|January 28, 2020
Benign hereditary chorea: From benign to seriousA Lamiral, S El Chehadeh, J Chelly, et al.
Biochemical and Biophysical Research Communications|July 31, 1991
Illegitimate (or ectopic) transcription proceeds through the usual promotersJ Chelly, J P Hugnot, J P Concordet, et al.
Cell|June 17, 1994
Isolation of the gene for McLeod syndrome that encodes a novel membrane transport proteinM Ho, J Chelly, N Carter, et al.
Annales De L'Anesthesiologie Francaise|January 1, 1979
[Anesthesia for aorto-coronary bypass]B Fontaine, E Bertrandias, D Tournay, et al.
Genomics|April 10, 1995
Characterization of the exon structure of the Menkes disease gene using vectorette PCRZ Tümer, B Vural, T Tønnesen, et al.
Revue Neurologique|January 18, 2021
Paroxysmal dyskinesia: When a PRRT2 variant hides a curable causeV Schneider, M Ferrari-Henquinet, A O Diallo, et al.
European Journal of Biochemistry|February 14, 1990
Quantitative estimation of minor mRNAs by cDNA-polymerase chain reaction. Application to dystrophin mRNA in cultured myogenic and brain cellsJ Chelly, D Montarras, C Pinset, et al.
Human Genetics|December 1, 1987
Familial deletion of Xp21.2 with glycerol kinase deficiency and congenital adrenal hypoplasiaF Marlhens, J Chelly, J C Kaplan, et al.
Journal of Medical Genetics|January 5, 2002
Evidence of somatic mosaicism for a MECP2 mutation in females with Rett syndrome: diagnostic implicationsV Bourdon, C Philippe, T Bienvenu, et al.
Pageof 16