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J L Knight

Showing results (71-80 of 108) with videos related to

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Leukemia|January 20, 2012
Quantification of subclonal distributions of recurrent genomic aberrations in paired pre-treatment and relapse samples from patients with B-cell chronic lymphocytic leukemiaS J L Knight, C Yau, R Clifford, et al.
British Journal of Haematology|May 30, 2018
Clinical-grade validation of whole genome sequencing reveals robust detection of low-frequency variants and copy number alterations in CLLJenny Klintman, Katerina Barmpouti, Samantha J L Knight, et al.
American Journal of Medical Genetics. Part A|October 16, 2010
Phenotype and natural history in Marshall-Smith syndromeAdam C Shaw, Inge D C van Balkom, Mislen Bauer, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 31, 2019
The complete costs of genome sequencing: a microcosting study in cancer and rare diseases from a single center in the United KingdomKatharina Schwarze, James Buchanan, Jilles M Fermont, et al.
Journal of Medical Genetics|September 18, 2014
De novo and rare inherited mutations implicate the transcriptional coregulator TCF20/SPBP in autism spectrum disorderChristian Babbs, Deborah Lloyd, Alistair T Pagnamenta, et al.
Nucleic Acids Research|June 18, 2005
SW-ARRAY: a dynamic programming solution for the identification of copy-number changes in genomic DNA using array comparative genome hybridization dataThomas S Price, Regina Regan, Richard Mott, et al.
Blood|November 18, 2020
Genomic and transcriptomic correlates of Richter transformation in chronic lymphocytic leukemiaJenny Klintman, Niamh Appleby, Basile Stamatopoulos, et al.
European Journal of Human Genetics : EJHG|December 27, 2007
Identification of non-recurrent submicroscopic genome imbalances: the advantage of genome-wide microarrays over targeted approachesDavid A Koolen, Erik A Sistermans, Willy Nilessen, et al.
American Journal of Human Genetics|October 16, 2012
Mutations in multidomain protein MEGF8 identify a Carpenter syndrome subtype associated with defective lateralizationStephen R F Twigg, Deborah Lloyd, Dagan Jenkins, et al.
Leukemia|November 22, 2017
Whole-genome sequencing of chronic lymphocytic leukaemia reveals distinct differences in the mutational landscape between IgHV<sup>mut</sup> and IgHV<sup>unmut</sup> subgroupsA Burns, R Alsolami, J Becq, et al.
Pageof 11

Showing results (71-80 of 108) with videos related to

Sort By:
Pageof 11
Leukemia|January 20, 2012
Quantification of subclonal distributions of recurrent genomic aberrations in paired pre-treatment and relapse samples from patients with B-cell chronic lymphocytic leukemiaS J L Knight, C Yau, R Clifford, et al.
British Journal of Haematology|May 30, 2018
Clinical-grade validation of whole genome sequencing reveals robust detection of low-frequency variants and copy number alterations in CLLJenny Klintman, Katerina Barmpouti, Samantha J L Knight, et al.
American Journal of Medical Genetics. Part A|October 16, 2010
Phenotype and natural history in Marshall-Smith syndromeAdam C Shaw, Inge D C van Balkom, Mislen Bauer, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 31, 2019
The complete costs of genome sequencing: a microcosting study in cancer and rare diseases from a single center in the United KingdomKatharina Schwarze, James Buchanan, Jilles M Fermont, et al.
Journal of Medical Genetics|September 18, 2014
De novo and rare inherited mutations implicate the transcriptional coregulator TCF20/SPBP in autism spectrum disorderChristian Babbs, Deborah Lloyd, Alistair T Pagnamenta, et al.
Nucleic Acids Research|June 18, 2005
SW-ARRAY: a dynamic programming solution for the identification of copy-number changes in genomic DNA using array comparative genome hybridization dataThomas S Price, Regina Regan, Richard Mott, et al.
Blood|November 18, 2020
Genomic and transcriptomic correlates of Richter transformation in chronic lymphocytic leukemiaJenny Klintman, Niamh Appleby, Basile Stamatopoulos, et al.
European Journal of Human Genetics : EJHG|December 27, 2007
Identification of non-recurrent submicroscopic genome imbalances: the advantage of genome-wide microarrays over targeted approachesDavid A Koolen, Erik A Sistermans, Willy Nilessen, et al.
American Journal of Human Genetics|October 16, 2012
Mutations in multidomain protein MEGF8 identify a Carpenter syndrome subtype associated with defective lateralizationStephen R F Twigg, Deborah Lloyd, Dagan Jenkins, et al.
Leukemia|November 22, 2017
Whole-genome sequencing of chronic lymphocytic leukaemia reveals distinct differences in the mutational landscape between IgHV<sup>mut</sup> and IgHV<sup>unmut</sup> subgroupsA Burns, R Alsolami, J Becq, et al.
Pageof 11