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Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
March 15, 2014
Identity-by-descent-guided mutation analysis and exome sequencing in consanguineous families reveals unusual clinical and molecular findings in retinal dystrophy
Frauke Coppieters, Kristof Van Schil, Miriam Bauwens, et al.
Plos One
|
October 8, 2011
Practical tools to implement massive parallel pyrosequencing of PCR products in next generation molecular diagnostics
Kim De Leeneer, Joachim De Schrijver, Lieven Clement, et al.
Scientific Reports
|
July 18, 2019
Author Correction: Integrative analysis identifies lincRNAs up- and downstream of neuroblastoma driver genes
Dries Rombaut, Hua-Sheng Chiu, Bieke Decaesteker, et al.
Scientific Reports
|
April 7, 2019
Integrative analysis identifies lincRNAs up- and downstream of neuroblastoma driver genes
Dries Rombaut, Hua-Sheng Chiu, Bieke Decaesteker, et al.
BMC Medical Genomics
|
May 22, 2012
Molecular diagnostics for congenital hearing loss including 15 deafness genes using a next generation sequencing platform
Sarah De Keulenaer, Jan Hellemans, Steve Lefever, et al.
Oncotarget
|
March 2, 2018
The mutational landscape of <i>MYCN</i>, <i>Lin28b</i> and <i>ALK</i><sup></sup> driven murine neuroblastoma mimics human disease
Bram De Wilde, Anneleen Beckers, Sven Lindner, et al.
International Journal of Molecular Sciences
|
October 14, 2022
mRNA Capture Sequencing and RT-qPCR for the Detection of Pathognomonic, Novel, and Secondary Fusion Transcripts in FFPE Tissue: A Sarcoma Showcase
Anneleen Decock, David Creytens, Steve Lefever, et al.
Plos One
|
January 12, 2013
Focal DNA copy number changes in neuroblastoma target MYCN regulated genes
Candy Kumps, Annelies Fieuw, Pieter Mestdagh, et al.
Genes, Chromosomes & Cancer
|
December 18, 2020
Recurrent chromosomal imbalances provide selective advantage to human embryonic stem cells under enhanced replicative stress conditions
Liselot M Mus, Stéphane Van Haver, Mina Popovic, et al.
Cell Reports
|
December 30, 2020
Charting Extracellular Transcriptomes in The Human Biofluid RNA Atlas
Eva Hulstaert, Annelien Morlion, Francisco Avila Cobos, et al.
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Showing results (41-50 of 54) with videos related to
Sort By:
Page
of 6
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
March 15, 2014
Identity-by-descent-guided mutation analysis and exome sequencing in consanguineous families reveals unusual clinical and molecular findings in retinal dystrophy
Frauke Coppieters, Kristof Van Schil, Miriam Bauwens, et al.
Plos One
|
October 8, 2011
Practical tools to implement massive parallel pyrosequencing of PCR products in next generation molecular diagnostics
Kim De Leeneer, Joachim De Schrijver, Lieven Clement, et al.
Scientific Reports
|
July 18, 2019
Author Correction: Integrative analysis identifies lincRNAs up- and downstream of neuroblastoma driver genes
Dries Rombaut, Hua-Sheng Chiu, Bieke Decaesteker, et al.
Scientific Reports
|
April 7, 2019
Integrative analysis identifies lincRNAs up- and downstream of neuroblastoma driver genes
Dries Rombaut, Hua-Sheng Chiu, Bieke Decaesteker, et al.
BMC Medical Genomics
|
May 22, 2012
Molecular diagnostics for congenital hearing loss including 15 deafness genes using a next generation sequencing platform
Sarah De Keulenaer, Jan Hellemans, Steve Lefever, et al.
Oncotarget
|
March 2, 2018
The mutational landscape of <i>MYCN</i>, <i>Lin28b</i> and <i>ALK</i><sup></sup> driven murine neuroblastoma mimics human disease
Bram De Wilde, Anneleen Beckers, Sven Lindner, et al.
International Journal of Molecular Sciences
|
October 14, 2022
mRNA Capture Sequencing and RT-qPCR for the Detection of Pathognomonic, Novel, and Secondary Fusion Transcripts in FFPE Tissue: A Sarcoma Showcase
Anneleen Decock, David Creytens, Steve Lefever, et al.
Plos One
|
January 12, 2013
Focal DNA copy number changes in neuroblastoma target MYCN regulated genes
Candy Kumps, Annelies Fieuw, Pieter Mestdagh, et al.
Genes, Chromosomes & Cancer
|
December 18, 2020
Recurrent chromosomal imbalances provide selective advantage to human embryonic stem cells under enhanced replicative stress conditions
Liselot M Mus, Stéphane Van Haver, Mina Popovic, et al.
Cell Reports
|
December 30, 2020
Charting Extracellular Transcriptomes in The Human Biofluid RNA Atlas
Eva Hulstaert, Annelien Morlion, Francisco Avila Cobos, et al.
Page
of 6