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J Taft

Showing results (261-270 of 318) with videos related to

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Medrxiv : the Preprint Server for Health Sciences|April 8, 2024
Data-driven consideration of genetic disorders for global genomic newborn screening programsThomas Minten, Sarah Bick, Sophia Adelson, et al.
Neurology|August 3, 2014
TUBB4A de novo mutations cause isolated hypomyelinationAmy Pizzino, Tyler Mark Pierson, Yiran Guo, et al.
Plos Biology|July 19, 2011
The reality of pervasive transcriptionMichael B Clark, Paulo P Amaral, Felix J Schlesinger, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 21, 2018
Microdeletions excluding YWHAE and PAFAH1B1 cause a unique leukoencephalopathy: further delineation of the 17p13.3 microdeletion spectrumLisa T Emrick, Jill A Rosenfeld, Seema R Lalani, et al.
BMC Genomics|April 22, 2009
A transcriptional sketch of a primary human breast cancer by 454 deep sequencingAlessandro Guffanti, Michele Iacono, Paride Pelucchi, et al.
Pediatric Neurology|June 10, 2021
Further Delineation of the Clinical and Pathologic Features of HIKESHI-Related Hypomyelinating LeukodystrophyGuy Helman, Ayelet Zerem, Akshata Almad, et al.
American Journal of Respiratory and Critical Care Medicine|October 31, 2013
Air trapping and airflow obstruction in newborn cystic fibrosis pigletsRyan J Adam, Andrew S Michalski, Christian Bauer, et al.
Pediatric Neurology|May 11, 2020
Phenotypic and Imaging Spectrum Associated With WDR45Laura A Adang, Amy Pizzino, Alka Malhotra, et al.
NPJ Genomic Medicine|October 28, 2020
Best practices for the analytical validation of clinical whole-genome sequencing intended for the diagnosis of germline diseaseChristian R Marshall, Shimul Chowdhury, Ryan J Taft, et al.
NPJ Genomic Medicine|October 29, 2024
Clinical genome sequencing in patients with suspected rare genetic disease in PeruJeny Bazalar-Montoya, Mario Cornejo-Olivas, Milagros M Duenas-Roque, et al.
Pageof 32

Showing results (261-270 of 318) with videos related to

Sort By:
Pageof 32
Medrxiv : the Preprint Server for Health Sciences|April 8, 2024
Data-driven consideration of genetic disorders for global genomic newborn screening programsThomas Minten, Sarah Bick, Sophia Adelson, et al.
Neurology|August 3, 2014
TUBB4A de novo mutations cause isolated hypomyelinationAmy Pizzino, Tyler Mark Pierson, Yiran Guo, et al.
Plos Biology|July 19, 2011
The reality of pervasive transcriptionMichael B Clark, Paulo P Amaral, Felix J Schlesinger, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 21, 2018
Microdeletions excluding YWHAE and PAFAH1B1 cause a unique leukoencephalopathy: further delineation of the 17p13.3 microdeletion spectrumLisa T Emrick, Jill A Rosenfeld, Seema R Lalani, et al.
BMC Genomics|April 22, 2009
A transcriptional sketch of a primary human breast cancer by 454 deep sequencingAlessandro Guffanti, Michele Iacono, Paride Pelucchi, et al.
Pediatric Neurology|June 10, 2021
Further Delineation of the Clinical and Pathologic Features of HIKESHI-Related Hypomyelinating LeukodystrophyGuy Helman, Ayelet Zerem, Akshata Almad, et al.
American Journal of Respiratory and Critical Care Medicine|October 31, 2013
Air trapping and airflow obstruction in newborn cystic fibrosis pigletsRyan J Adam, Andrew S Michalski, Christian Bauer, et al.
Pediatric Neurology|May 11, 2020
Phenotypic and Imaging Spectrum Associated With WDR45Laura A Adang, Amy Pizzino, Alka Malhotra, et al.
NPJ Genomic Medicine|October 28, 2020
Best practices for the analytical validation of clinical whole-genome sequencing intended for the diagnosis of germline diseaseChristian R Marshall, Shimul Chowdhury, Ryan J Taft, et al.
NPJ Genomic Medicine|October 29, 2024
Clinical genome sequencing in patients with suspected rare genetic disease in PeruJeny Bazalar-Montoya, Mario Cornejo-Olivas, Milagros M Duenas-Roque, et al.
Pageof 32