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The American Journal of Psychiatry
|
May 2, 2018
Developmental Delay, Treatment-Resistant Psychosis, and Early-Onset Dementia in a Man With 22q11 Deletion Syndrome and Huntington's Disease
Martilias Farrell, Maya Lichtenstein, James J Crowley, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
April 17, 2008
Microduplications of 22q11.2 are frequently inherited and are associated with variable phenotypes
Zhishuo Ou, Jonathan S Berg, Hagith Yonath, et al.
BMC Bioinformatics
|
July 21, 2021
Pre-capture multiplexing provides additional power to detect copy number variation in exome sequencing
Dayne L Filer, Fengshen Kuo, Alicia T Brandt, et al.
Personalized Medicine
|
October 7, 2020
Engaging community stakeholders in research on best practices for clinical genomic sequencing
Ida Griesemer, Brooke S Staley, Alexandra F Lightfoot, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
February 2, 2018
Anticipated responses of early adopter genetic specialists and nongenetic specialists to unsolicited genomic secondary findings
Kurt D Christensen, Barbara A Bernhardt, Gail P Jarvik, et al.
Schizophrenia Research
|
September 18, 2020
Treatment-resistant psychotic symptoms and early-onset dementia: A case report of the 3q29 deletion syndrome
Matthew K Harner, Maya Lichtenstein, Martilias Farrell, et al.
Nature Genetics
|
December 6, 2011
Dnmt3a is essential for hematopoietic stem cell differentiation
Grant A Challen, Deqiang Sun, Mira Jeong, et al.
Translational Psychiatry
|
February 19, 2020
Treatment-resistant psychotic symptoms and the 15q11.2 BP1-BP2 (Burnside-Butler) deletion syndrome: case report and review of the literature
Martilias Farrell, Maya Lichtenstein, Matthew K Harner, et al.
Journal of Clinical and Translational Science
|
April 10, 2026
Expanding access to genomic analysis and reporting in research studies: The GENYSIS research core
Kimberly S Foss, Tam P Sneddon, Eleanor P Fensterle, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 22, 2013
ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing
Robert C Green, Jonathan S Berg, Wayne W Grody, et al.
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Search research articles
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Showing results (101-110 of 168) with videos related to
Sort By:
Page
of 17
The American Journal of Psychiatry
|
May 2, 2018
Developmental Delay, Treatment-Resistant Psychosis, and Early-Onset Dementia in a Man With 22q11 Deletion Syndrome and Huntington's Disease
Martilias Farrell, Maya Lichtenstein, James J Crowley, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
April 17, 2008
Microduplications of 22q11.2 are frequently inherited and are associated with variable phenotypes
Zhishuo Ou, Jonathan S Berg, Hagith Yonath, et al.
BMC Bioinformatics
|
July 21, 2021
Pre-capture multiplexing provides additional power to detect copy number variation in exome sequencing
Dayne L Filer, Fengshen Kuo, Alicia T Brandt, et al.
Personalized Medicine
|
October 7, 2020
Engaging community stakeholders in research on best practices for clinical genomic sequencing
Ida Griesemer, Brooke S Staley, Alexandra F Lightfoot, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
February 2, 2018
Anticipated responses of early adopter genetic specialists and nongenetic specialists to unsolicited genomic secondary findings
Kurt D Christensen, Barbara A Bernhardt, Gail P Jarvik, et al.
Schizophrenia Research
|
September 18, 2020
Treatment-resistant psychotic symptoms and early-onset dementia: A case report of the 3q29 deletion syndrome
Matthew K Harner, Maya Lichtenstein, Martilias Farrell, et al.
Nature Genetics
|
December 6, 2011
Dnmt3a is essential for hematopoietic stem cell differentiation
Grant A Challen, Deqiang Sun, Mira Jeong, et al.
Translational Psychiatry
|
February 19, 2020
Treatment-resistant psychotic symptoms and the 15q11.2 BP1-BP2 (Burnside-Butler) deletion syndrome: case report and review of the literature
Martilias Farrell, Maya Lichtenstein, Matthew K Harner, et al.
Journal of Clinical and Translational Science
|
April 10, 2026
Expanding access to genomic analysis and reporting in research studies: The GENYSIS research core
Kimberly S Foss, Tam P Sneddon, Eleanor P Fensterle, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 22, 2013
ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing
Robert C Green, Jonathan S Berg, Wayne W Grody, et al.
Page
of 17