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Catherine E Cottrell

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Pediatric Blood & Cancer|October 25, 2023
Fatal brainstem injury following proton radiation in a patient with medulloblastoma and a germline variant in RNF213Darren M Klawinski, Catherine E Cottrell, Kathleen M Schieffer, et al.
Life (Basel, Switzerland)|March 28, 2024
Structural and Dynamic Analyses of Pathogenic Variants in <i>PIK3R1</i> Reveal a Shared Mechanism Associated among Cancer, Undergrowth, and Overgrowth SyndromesNikita R Dsouza, Catherine E Cottrell, Olivia M T Davies, et al.
Neuro-Oncology Advances|January 12, 2024
A LINE-1 mediated deletion resulting in germline retinoblastoma predispositionErica L Macke, Anthony R Miller, Eileen Stonerock, et al.
Case Reports in Dermatological Medicine|February 14, 2022
Syringocystadenocarcinoma Papilliferum in a Fifteen-Year-Old Girl: A Case Report and Review of the LiteratureJordan N Halsey, Esteban Fernandez Faith, Suzanna J Logan, et al.
JAMA Dermatology|March 9, 2018
Scarring in Patients With PIK3CA-Related Overgrowth SyndromesJack E Steiner, Catherine E Cottrell, Jenna L Streicher, et al.
Plos One|September 3, 2015
Identification of Medically Actionable Secondary Findings in the 1000 GenomesEmily Olfson, Catherine E Cottrell, Nicholas O Davidson, et al.
Muscle & Nerve|October 4, 2023
Exome sequencing in the pediatric neuromuscular clinic leads to more frequent diagnosis of both neuromuscular and neurodevelopmental conditionsAlayne P Meyer, Jianing Ma, Guy Brock, et al.
The Journal of Molecular Diagnostics : JMD|May 13, 2014
Detection of gene rearrangements in targeted clinical next-generation sequencingHaley J Abel, Hussam Al-Kateb, Catherine E Cottrell, et al.
Pediatric Dermatology|November 28, 2022
Early-onset hypertension associated with extensive cutaneous capillary malformations harboring postzygotic variants in GNAQ and GNA11Olivia M T Davies, Ashley T Ng, Jennifer Tran, et al.
Cold Spring Harbor Molecular Case Studies|October 30, 2021
Somatic variation as an incidental finding in the pediatric next-generation sequencing eraMarilena Melas, Mariam T Mathew, Mari Mori, et al.
Pageof 8

Showing results (21-30 of 72) with videos related to

Sort By:
Pageof 8
Pediatric Blood & Cancer|October 25, 2023
Fatal brainstem injury following proton radiation in a patient with medulloblastoma and a germline variant in RNF213Darren M Klawinski, Catherine E Cottrell, Kathleen M Schieffer, et al.
Life (Basel, Switzerland)|March 28, 2024
Structural and Dynamic Analyses of Pathogenic Variants in <i>PIK3R1</i> Reveal a Shared Mechanism Associated among Cancer, Undergrowth, and Overgrowth SyndromesNikita R Dsouza, Catherine E Cottrell, Olivia M T Davies, et al.
Neuro-Oncology Advances|January 12, 2024
A LINE-1 mediated deletion resulting in germline retinoblastoma predispositionErica L Macke, Anthony R Miller, Eileen Stonerock, et al.
Case Reports in Dermatological Medicine|February 14, 2022
Syringocystadenocarcinoma Papilliferum in a Fifteen-Year-Old Girl: A Case Report and Review of the LiteratureJordan N Halsey, Esteban Fernandez Faith, Suzanna J Logan, et al.
JAMA Dermatology|March 9, 2018
Scarring in Patients With PIK3CA-Related Overgrowth SyndromesJack E Steiner, Catherine E Cottrell, Jenna L Streicher, et al.
Plos One|September 3, 2015
Identification of Medically Actionable Secondary Findings in the 1000 GenomesEmily Olfson, Catherine E Cottrell, Nicholas O Davidson, et al.
Muscle & Nerve|October 4, 2023
Exome sequencing in the pediatric neuromuscular clinic leads to more frequent diagnosis of both neuromuscular and neurodevelopmental conditionsAlayne P Meyer, Jianing Ma, Guy Brock, et al.
The Journal of Molecular Diagnostics : JMD|May 13, 2014
Detection of gene rearrangements in targeted clinical next-generation sequencingHaley J Abel, Hussam Al-Kateb, Catherine E Cottrell, et al.
Pediatric Dermatology|November 28, 2022
Early-onset hypertension associated with extensive cutaneous capillary malformations harboring postzygotic variants in GNAQ and GNA11Olivia M T Davies, Ashley T Ng, Jennifer Tran, et al.
Cold Spring Harbor Molecular Case Studies|October 30, 2021
Somatic variation as an incidental finding in the pediatric next-generation sequencing eraMarilena Melas, Mariam T Mathew, Mari Mori, et al.
Pageof 8