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W Scherer

Showing results (341-350 of 915) with videos related to

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Plos Genetics|April 26, 2008
SNPs meet CNVs in genome-wide association studies: HGV2007 meeting reportXavier Estivill, Nancy J Cox, Stephen J Chanock, et al.
The Cochrane Database of Systematic Reviews|March 13, 2023
Medical interventions for traumatic hyphemaFasika A Woreta, Kristina B Lindsley, Almutez Gharaibeh, et al.
European Journal of Human Genetics : EJHG|February 23, 2026
Flexible and rapid validation of structural variation using adaptive samplingAida Paivandy, Felix Lenner, Jesper Eisfeldt, et al.
Contemporary Clinical Trials|February 4, 2021
National Institute of Mental Health Recruitment Monitoring Policy and Clinical Trial ImpactEugene I Kane, Gail L Daumit, Kevin M Fain, et al.
Genome Biology|April 19, 2003
Genome-wide detection of segmental duplications and potential assembly errors in the human genome sequenceJoseph Cheung, Xavier Estivill, Razi Khaja, et al.
Genomics|November 5, 1997
PMS2-related genes flank the rearrangement breakpoints associated with Williams syndrome and other diseases on human chromosome 7L R Osborne, J A Herbrick, T Greavette, et al.
Genomics|April 1, 1997
The XRCC2 DNA repair gene: identification of a positional candidateC E Tambini, A M George, J M Rommens, et al.
European Journal of Human Genetics : EJHG|September 6, 2022
Developmental implications of genetic testing for physical indicationsDanielle A Baribeau, Ny Hoang, Thanuja Selvanayagam, et al.
G3 (Bethesda, Md.)|November 7, 2013
Performance of high-throughput sequencing for the discovery of genetic variation across the complete size spectrumAndy Wing Chun Pang, Jeffrey R Macdonald, Ryan K C Yuen, et al.
Ophthalmology. Retina|August 27, 2023
Terminology for Retinal Findings in Sickle Cell Disease Research: A Scoping ReviewGrace R Reilly, Yangyiran Xie, Roberta W Scherer, et al.
Pageof 92

Showing results (341-350 of 915) with videos related to

Sort By:
Pageof 92
Plos Genetics|April 26, 2008
SNPs meet CNVs in genome-wide association studies: HGV2007 meeting reportXavier Estivill, Nancy J Cox, Stephen J Chanock, et al.
The Cochrane Database of Systematic Reviews|March 13, 2023
Medical interventions for traumatic hyphemaFasika A Woreta, Kristina B Lindsley, Almutez Gharaibeh, et al.
European Journal of Human Genetics : EJHG|February 23, 2026
Flexible and rapid validation of structural variation using adaptive samplingAida Paivandy, Felix Lenner, Jesper Eisfeldt, et al.
Contemporary Clinical Trials|February 4, 2021
National Institute of Mental Health Recruitment Monitoring Policy and Clinical Trial ImpactEugene I Kane, Gail L Daumit, Kevin M Fain, et al.
Genome Biology|April 19, 2003
Genome-wide detection of segmental duplications and potential assembly errors in the human genome sequenceJoseph Cheung, Xavier Estivill, Razi Khaja, et al.
Genomics|November 5, 1997
PMS2-related genes flank the rearrangement breakpoints associated with Williams syndrome and other diseases on human chromosome 7L R Osborne, J A Herbrick, T Greavette, et al.
Genomics|April 1, 1997
The XRCC2 DNA repair gene: identification of a positional candidateC E Tambini, A M George, J M Rommens, et al.
European Journal of Human Genetics : EJHG|September 6, 2022
Developmental implications of genetic testing for physical indicationsDanielle A Baribeau, Ny Hoang, Thanuja Selvanayagam, et al.
G3 (Bethesda, Md.)|November 7, 2013
Performance of high-throughput sequencing for the discovery of genetic variation across the complete size spectrumAndy Wing Chun Pang, Jeffrey R Macdonald, Ryan K C Yuen, et al.
Ophthalmology. Retina|August 27, 2023
Terminology for Retinal Findings in Sickle Cell Disease Research: A Scoping ReviewGrace R Reilly, Yangyiran Xie, Roberta W Scherer, et al.
Pageof 92