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Francesco Vezzi

Showing results (21-30 of 27) with videos related to

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Journal of Medical Genetics|December 5, 2014
CTNND2-a candidate gene for reading problems and mild intellectual disabilityWolfgang Hofmeister, Daniel Nilsson, Alexandra Topa, et al.
The European Respiratory Journal|November 21, 2015
T-cell receptor-HLA-DRB1 associations suggest specific antigens in pulmonary sarcoidosisJohan Grunewald, Ylva Kaiser, Mahyar Ostadkarampour, et al.
Human Mutation|November 19, 2016
Whole-Genome Sequencing of Cytogenetically Balanced Chromosome Translocations Identifies Potentially Pathological Gene Disruptions and Highlights the Importance of Microhomology in the Mechanism of FormationDaniel Nilsson, Maria Pettersson, Peter Gustavsson, et al.
Plos Genetics|November 13, 2018
Replicative and non-replicative mechanisms in the formation of clustered CNVs are indicated by whole genome characterizationLusine Nazaryan-Petersen, Jesper Eisfeldt, Maria Pettersson, et al.
European Journal of Human Genetics : EJHG|August 24, 2017
SweGen: a whole-genome data resource of genetic variability in a cross-section of the Swedish populationAdam Ameur, Johan Dahlberg, Pall Olason, et al.
Nature|May 24, 2013
The Norway spruce genome sequence and conifer genome evolutionBjörn Nystedt, Nathaniel R Street, Anna Wetterbom, et al.
Gigascience|July 23, 2013
Assemblathon 2: evaluating de novo methods of genome assembly in three vertebrate speciesKeith R Bradnam, Joseph N Fass, Anton Alexandrov, et al.
Pageof 3

Showing results (21-30 of 27) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 27 results.
Journal of Medical Genetics|December 5, 2014
CTNND2-a candidate gene for reading problems and mild intellectual disabilityWolfgang Hofmeister, Daniel Nilsson, Alexandra Topa, et al.
The European Respiratory Journal|November 21, 2015
T-cell receptor-HLA-DRB1 associations suggest specific antigens in pulmonary sarcoidosisJohan Grunewald, Ylva Kaiser, Mahyar Ostadkarampour, et al.
Human Mutation|November 19, 2016
Whole-Genome Sequencing of Cytogenetically Balanced Chromosome Translocations Identifies Potentially Pathological Gene Disruptions and Highlights the Importance of Microhomology in the Mechanism of FormationDaniel Nilsson, Maria Pettersson, Peter Gustavsson, et al.
Plos Genetics|November 13, 2018
Replicative and non-replicative mechanisms in the formation of clustered CNVs are indicated by whole genome characterizationLusine Nazaryan-Petersen, Jesper Eisfeldt, Maria Pettersson, et al.
European Journal of Human Genetics : EJHG|August 24, 2017
SweGen: a whole-genome data resource of genetic variability in a cross-section of the Swedish populationAdam Ameur, Johan Dahlberg, Pall Olason, et al.
Nature|May 24, 2013
The Norway spruce genome sequence and conifer genome evolutionBjörn Nystedt, Nathaniel R Street, Anna Wetterbom, et al.
Gigascience|July 23, 2013
Assemblathon 2: evaluating de novo methods of genome assembly in three vertebrate speciesKeith R Bradnam, Joseph N Fass, Anton Alexandrov, et al.
Pageof 3