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Plos Genetics
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April 26, 2008
SNPs meet CNVs in genome-wide association studies: HGV2007 meeting report
Xavier Estivill, Nancy J Cox, Stephen J Chanock, et al.
The Cochrane Database of Systematic Reviews
|
March 13, 2023
Medical interventions for traumatic hyphema
Fasika 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 sampling
Aida Paivandy, Felix Lenner, Jesper Eisfeldt, et al.
Contemporary Clinical Trials
|
February 4, 2021
National Institute of Mental Health Recruitment Monitoring Policy and Clinical Trial Impact
Eugene 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 sequence
Joseph 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 7
L R Osborne, J A Herbrick, T Greavette, et al.
Genomics
|
April 1, 1997
The XRCC2 DNA repair gene: identification of a positional candidate
C 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 indications
Danielle 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 spectrum
Andy 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 Review
Grace R Reilly, Yangyiran Xie, Roberta W Scherer, et al.
Page
of 92
Search research articles
Search
Showing results (341-350 of 915) with videos related to
Sort By:
Page
of 92
Plos Genetics
|
April 26, 2008
SNPs meet CNVs in genome-wide association studies: HGV2007 meeting report
Xavier Estivill, Nancy J Cox, Stephen J Chanock, et al.
The Cochrane Database of Systematic Reviews
|
March 13, 2023
Medical interventions for traumatic hyphema
Fasika 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 sampling
Aida Paivandy, Felix Lenner, Jesper Eisfeldt, et al.
Contemporary Clinical Trials
|
February 4, 2021
National Institute of Mental Health Recruitment Monitoring Policy and Clinical Trial Impact
Eugene 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 sequence
Joseph 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 7
L R Osborne, J A Herbrick, T Greavette, et al.
Genomics
|
April 1, 1997
The XRCC2 DNA repair gene: identification of a positional candidate
C 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 indications
Danielle 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 spectrum
Andy 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 Review
Grace R Reilly, Yangyiran Xie, Roberta W Scherer, et al.
Page
of 92