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A Totaro

Showing results (81-90 of 89) with videos related to

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American Journal of Human Genetics|March 1, 1997
Localization, by linkage analysis, of the cystinuria type III gene to chromosome 19q13.1L Bisceglia, M J Calonge, A Totaro, et al.
Colorectal Disease : the Official Journal of the Association of Coloproctology of Great Britain and Ireland|September 7, 2020
Changing paradigm of sacral neuromodulation and external anal sphincter repair for faecal incontinence in specialist centresK Ong, L Bordeianou, M Brunner, et al.
European Journal of Human Genetics : EJHG|March 1, 1997
Linkage of DFNB1 to non-syndromic neurosensory autosomal-recessive deafness in Mediterranean familiesP Gasparini, X Estivill, V Volpini, et al.
Journal of Medicinal Chemistry|October 1, 1979
Synthesis, assignment of absolute configuration, and receptor binding studies relevant to the neuroleptic activities of a series of chiral 3-substituted cyproheptadine atropisomersW C Randall, P S Anderson, E L Cresson, et al.
Journal of Medical Genetics|September 6, 2005
Extensive scanning of the calpain-3 gene broadens the spectrum of LGMD2A phenotypesG Piluso, L Politano, S Aurino, et al.
Journal of Medicinal Chemistry|July 1, 1983
Synthesis and receptor binding studies relevant to the neuroleptic activities of some 1-methyl-4-piperidylidene-9-substituted-pyrrolo[2,1-b][3]benzazepine derivativesD C Remy, S F Britcher, S W King, et al.
Nature Communications|July 21, 2021
Fully automated fast-flow synthesis of antisense phosphorodiamidate morpholino oligomersChengxi Li, Alex J Callahan, Mark D Simon, et al.
Molecular Psychiatry|April 24, 2001
Reelin gene alleles and haplotypes as a factor predisposing to autistic disorderA M Persico, L D'Agruma, N Maiorano, et al.
Nature Genetics|November 5, 1999
Polymorphism in intron 4 of HFE does not compromise haemochromatosis mutation results. The European Haemochromatosis ConsortiumA T Merryweather-Clarke, J J Pointon, J D Shearman, et al.
Pageof 9

Showing results (81-90 of 89) with videos related to

Sort By:
Pageof 9
You have reached the last page of results.This site can display upto 89 results.
American Journal of Human Genetics|March 1, 1997
Localization, by linkage analysis, of the cystinuria type III gene to chromosome 19q13.1L Bisceglia, M J Calonge, A Totaro, et al.
Colorectal Disease : the Official Journal of the Association of Coloproctology of Great Britain and Ireland|September 7, 2020
Changing paradigm of sacral neuromodulation and external anal sphincter repair for faecal incontinence in specialist centresK Ong, L Bordeianou, M Brunner, et al.
European Journal of Human Genetics : EJHG|March 1, 1997
Linkage of DFNB1 to non-syndromic neurosensory autosomal-recessive deafness in Mediterranean familiesP Gasparini, X Estivill, V Volpini, et al.
Journal of Medicinal Chemistry|October 1, 1979
Synthesis, assignment of absolute configuration, and receptor binding studies relevant to the neuroleptic activities of a series of chiral 3-substituted cyproheptadine atropisomersW C Randall, P S Anderson, E L Cresson, et al.
Journal of Medical Genetics|September 6, 2005
Extensive scanning of the calpain-3 gene broadens the spectrum of LGMD2A phenotypesG Piluso, L Politano, S Aurino, et al.
Journal of Medicinal Chemistry|July 1, 1983
Synthesis and receptor binding studies relevant to the neuroleptic activities of some 1-methyl-4-piperidylidene-9-substituted-pyrrolo[2,1-b][3]benzazepine derivativesD C Remy, S F Britcher, S W King, et al.
Nature Communications|July 21, 2021
Fully automated fast-flow synthesis of antisense phosphorodiamidate morpholino oligomersChengxi Li, Alex J Callahan, Mark D Simon, et al.
Molecular Psychiatry|April 24, 2001
Reelin gene alleles and haplotypes as a factor predisposing to autistic disorderA M Persico, L D'Agruma, N Maiorano, et al.
Nature Genetics|November 5, 1999
Polymorphism in intron 4 of HFE does not compromise haemochromatosis mutation results. The European Haemochromatosis ConsortiumA T Merryweather-Clarke, J J Pointon, J D Shearman, et al.
Pageof 9