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American Journal of Medical Genetics. Part A
|
August 5, 2010
Copy number variation analysis in single-suture craniosynostosis: multiple rare variants including RUNX2 duplication in two cousins with metopic craniosynostosis
Heather C Mefford, Neil Shafer, Francesca Antonacci, et al.
Genes
|
July 2, 2021
Cytogenetic and Array-CGH Characterization of a Simple Case of Reciprocal t(3;10) Translocation Reveals a Hidden Deletion at 5q12
Angelo Cellamare, Nicoletta Coccaro, Maria Cristina Nuzzi, et al.
International Journal of Cancer
|
November 2, 2007
Identification of 2 putative critical segments of 17q gain in neuroblastoma through integrative genomics
Jo Vandesompele, Evi Michels, Katleen De Preter, et al.
Nature Genetics
|
September 1, 2009
Personalized copy number and segmental duplication maps using next-generation sequencing
Can Alkan, Jeffrey M Kidd, Tomas Marques-Bonet, et al.
Genome Research
|
January 15, 2014
Reconstructing complex regions of genomes using long-read sequencing technology
John Huddleston, Swati Ranade, Maika Malig, et al.
Nature
|
November 11, 2014
Resolving the complexity of the human genome using single-molecule sequencing
Mark J P Chaisson, John Huddleston, Megan Y Dennis, et al.
Genome Research
|
May 4, 2026
Single-cell template strand sequencing reveals culture-induced chromosomal instability in a gibbon cell line
Alessia Daponte, Gerardina Chirico, Annalisa Paparella, et al.
Nature Genetics
|
June 17, 2020
Recurrent inversion toggling and great ape genome evolution
David Porubsky, Ashley D Sanders, Wolfram Höps, et al.
Plos Genetics
|
March 28, 2019
Genomic inversions and GOLGA core duplicons underlie disease instability at the 15q25 locus
Flavia A M Maggiolini, Stuart Cantsilieris, Pietro D'Addabbo, et al.
Biorxiv : the Preprint Server for Biology
|
September 29, 2025
A complete and near-perfect rhesus macaque reference genome: lessons from subtelomeric repeats and sequencing bias
Shilong Zhang, Ning Xu, Yong Lu, et al.
Page
of 6
Search research articles
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Showing results (21-30 of 56) with videos related to
Sort By:
Page
of 6
American Journal of Medical Genetics. Part A
|
August 5, 2010
Copy number variation analysis in single-suture craniosynostosis: multiple rare variants including RUNX2 duplication in two cousins with metopic craniosynostosis
Heather C Mefford, Neil Shafer, Francesca Antonacci, et al.
Genes
|
July 2, 2021
Cytogenetic and Array-CGH Characterization of a Simple Case of Reciprocal t(3;10) Translocation Reveals a Hidden Deletion at 5q12
Angelo Cellamare, Nicoletta Coccaro, Maria Cristina Nuzzi, et al.
International Journal of Cancer
|
November 2, 2007
Identification of 2 putative critical segments of 17q gain in neuroblastoma through integrative genomics
Jo Vandesompele, Evi Michels, Katleen De Preter, et al.
Nature Genetics
|
September 1, 2009
Personalized copy number and segmental duplication maps using next-generation sequencing
Can Alkan, Jeffrey M Kidd, Tomas Marques-Bonet, et al.
Genome Research
|
January 15, 2014
Reconstructing complex regions of genomes using long-read sequencing technology
John Huddleston, Swati Ranade, Maika Malig, et al.
Nature
|
November 11, 2014
Resolving the complexity of the human genome using single-molecule sequencing
Mark J P Chaisson, John Huddleston, Megan Y Dennis, et al.
Genome Research
|
May 4, 2026
Single-cell template strand sequencing reveals culture-induced chromosomal instability in a gibbon cell line
Alessia Daponte, Gerardina Chirico, Annalisa Paparella, et al.
Nature Genetics
|
June 17, 2020
Recurrent inversion toggling and great ape genome evolution
David Porubsky, Ashley D Sanders, Wolfram Höps, et al.
Plos Genetics
|
March 28, 2019
Genomic inversions and GOLGA core duplicons underlie disease instability at the 15q25 locus
Flavia A M Maggiolini, Stuart Cantsilieris, Pietro D'Addabbo, et al.
Biorxiv : the Preprint Server for Biology
|
September 29, 2025
A complete and near-perfect rhesus macaque reference genome: lessons from subtelomeric repeats and sequencing bias
Shilong Zhang, Ning Xu, Yong Lu, et al.
Page
of 6