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Showing results (461-470 of 471) with videos related to

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Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 17, 2011
An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilitiesErin B Kaminsky, Vineith Kaul, Justin Paschall, et al.
Nature|May 10, 2002
Complete genome sequence of the model actinomycete Streptomyces coelicolor A3(2)S D Bentley, K F Chater, A-M Cerdeño-Tárraga, et al.
American Journal of Human Genetics|November 9, 2010
Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophreniaDaniel Moreno-De-Luca, , Jennifer G Mulle, et al.
Journal of Clinical Immunology|July 9, 2020
Neuroinflammatory Disease as an Isolated Manifestation of Hemophagocytic LymphohistiocytosisAnnaliesse Blincoe, Maximilian Heeg, Patrick K Campbell, et al.
Plos Genetics|March 14, 2012
A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility lociEimear E Kenny, Itsik Pe'er, Amir Karban, et al.
Nature|February 23, 2002
The genome sequence of Schizosaccharomyces pombeV Wood, R Gwilliam, M-A Rajandream, et al.
Molecular Psychiatry|February 5, 2020
Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletionIsabelle Cleynen, Worrawat Engchuan, Matthew S Hestand, et al.
Space Science Reviews|March 19, 2019
SEIS: Insight's Seismic Experiment for Internal Structure of MarsP Lognonné, W B Banerdt, D Giardini, et al.
Nature|March 17, 2006
The finished DNA sequence of human chromosome 12Steven E Scherer, Donna M Muzny, Christian J Buhay, et al.
Science (New York, N.Y.)|April 25, 2009
The genome sequence of taurine cattle: a window to ruminant biology and evolution, Christine G Elsik, Ross L Tellam, et al.
Pageof 48

Showing results (461-470 of 471) with videos related to

Sort By:
Pageof 48
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 17, 2011
An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilitiesErin B Kaminsky, Vineith Kaul, Justin Paschall, et al.
Nature|May 10, 2002
Complete genome sequence of the model actinomycete Streptomyces coelicolor A3(2)S D Bentley, K F Chater, A-M Cerdeño-Tárraga, et al.
American Journal of Human Genetics|November 9, 2010
Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophreniaDaniel Moreno-De-Luca, , Jennifer G Mulle, et al.
Journal of Clinical Immunology|July 9, 2020
Neuroinflammatory Disease as an Isolated Manifestation of Hemophagocytic LymphohistiocytosisAnnaliesse Blincoe, Maximilian Heeg, Patrick K Campbell, et al.
Plos Genetics|March 14, 2012
A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility lociEimear E Kenny, Itsik Pe'er, Amir Karban, et al.
Nature|February 23, 2002
The genome sequence of Schizosaccharomyces pombeV Wood, R Gwilliam, M-A Rajandream, et al.
Molecular Psychiatry|February 5, 2020
Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletionIsabelle Cleynen, Worrawat Engchuan, Matthew S Hestand, et al.
Space Science Reviews|March 19, 2019
SEIS: Insight's Seismic Experiment for Internal Structure of MarsP Lognonné, W B Banerdt, D Giardini, et al.
Nature|March 17, 2006
The finished DNA sequence of human chromosome 12Steven E Scherer, Donna M Muzny, Christian J Buhay, et al.
Science (New York, N.Y.)|April 25, 2009
The genome sequence of taurine cattle: a window to ruminant biology and evolution, Christine G Elsik, Ross L Tellam, et al.
Pageof 48