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Anesthesie, Analgesie, Reanimation|January 1, 1979
[Nitroglycerin and amyl nitrite action on common bile duct during operation for vesicular lithiasis (author's transl)]J Chelly, M L Tannières, D Tournay, 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.Genomics|September 1, 1994
DXS106 and DXS559 flank the X-linked dystonia-parkinsonism syndrome locus (DYT3)U Müller, G Haberhausen, T Wagner, et al.Nature|March 1, 1990
Dystrophin gene transcribed from different promoters in neuronal and glial cellsJ Chelly, G Hamard, A Koulakoff, et al.Neurology|November 9, 2000
Two affected boys in a Rett syndrome family: clinical and molecular findingsL Villard, A Kpebe, C Cardoso, et al.European Journal of Human Genetics : EJHG|April 21, 2001
Parental origin of de novo MECP2 mutations in Rett syndromeM Girard, P Couvert, A Carrié, et al.Anesthesie, Analgesie, Reanimation|January 1, 1979
[Prinzmetal's angina during myocardial revascularisation. Cardiovascular complications in 71 patients (author's transl)]B Fontaine, E Bertrandias, J Chelly, et al.European Journal of Human Genetics : EJHG|January 1, 1996
Analysis of alternative splicing patterns in the cystic fibrosis transmembrane conductance regulator gene using mRNA derived from lymphoblastoid cells of cystic fibrosis patientsT Bienvenu, C Beldjord, J Chelly, et al.European Journal of Human Genetics : EJHG|July 21, 2001
No mutations in the coding region of the Rett syndrome gene MECP2 in 59 autistic patientsP Vourc'h, T Bienvenu, C Beldjord, et al.Pageof 14