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Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
April 19, 2005
Detection and calibration of microdeletions and microduplications by array-based comparative genomic hybridization and its applicability to clinical genetic testing
Andrew Wong, Christa Lese Martin, Konstantina Heretis, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
September 18, 2007
The evolution of molecular ruler analysis for characterizing telomere imbalances: from fluorescence in situ hybridization to array comparative genomic hybridization
Christa Lese Martin, Zafar Nawaz, Erin L Baldwin, et al.
Genomics
|
July 6, 2004
Diverse fates of paralogs following segmental duplication of telomeric genes
Andrew Wong, Eric J Vallender, Konstantina Heretis, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
January 7, 2023
Phenotypic shift in copy number variants: Evidence in 16p11.2 duplication syndrome
Cora M Taylor, Brenda M Finucane, Andres Moreno-De-Luca, et al.
The Lancet. Neurology
|
March 23, 2013
Developmental brain dysfunction: revival and expansion of old concepts based on new genetic evidence
Andres Moreno-De-Luca, Scott M Myers, Thomas D Challman, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 19, 2021
Recontacting registry participants with genetic updates through GenomeConnect, the ClinGen patient registry
Juliann M Savatt, Danielle R Azzariti, David H Ledbetter, et al.
Plos One
|
June 22, 2012
Human preferences for symmetry: subjective experience, cognitive conflict and cortical brain activity
David W Evans, Patrick T Orr, Steven M Lazar, et al.
Human Molecular Genetics
|
May 16, 2009
Segmental duplications mediate novel, clinically relevant chromosome rearrangements
M Katharine Rudd, Julia Keene, Brian Bunke, et al.
Genomics
|
July 3, 2003
Complex low-copy repeats associated with a common polymorphic inversion at human chromosome 8p23
Hirobumi Sugawara, Naoki Harada, Tomoko Ida, et al.
JAMA Pediatrics
|
March 6, 2023
Diagnostic Yield of Exome Sequencing in Cerebral Palsy and Implications for Genetic Testing Guidelines: A Systematic Review and Meta-analysis
Pedro J Gonzalez-Mantilla, Yirui Hu, Scott M Myers, et al.
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of 13
Search research articles
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Showing results (31-40 of 125) with videos related to
Sort By:
Page
of 13
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
April 19, 2005
Detection and calibration of microdeletions and microduplications by array-based comparative genomic hybridization and its applicability to clinical genetic testing
Andrew Wong, Christa Lese Martin, Konstantina Heretis, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
September 18, 2007
The evolution of molecular ruler analysis for characterizing telomere imbalances: from fluorescence in situ hybridization to array comparative genomic hybridization
Christa Lese Martin, Zafar Nawaz, Erin L Baldwin, et al.
Genomics
|
July 6, 2004
Diverse fates of paralogs following segmental duplication of telomeric genes
Andrew Wong, Eric J Vallender, Konstantina Heretis, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
January 7, 2023
Phenotypic shift in copy number variants: Evidence in 16p11.2 duplication syndrome
Cora M Taylor, Brenda M Finucane, Andres Moreno-De-Luca, et al.
The Lancet. Neurology
|
March 23, 2013
Developmental brain dysfunction: revival and expansion of old concepts based on new genetic evidence
Andres Moreno-De-Luca, Scott M Myers, Thomas D Challman, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 19, 2021
Recontacting registry participants with genetic updates through GenomeConnect, the ClinGen patient registry
Juliann M Savatt, Danielle R Azzariti, David H Ledbetter, et al.
Plos One
|
June 22, 2012
Human preferences for symmetry: subjective experience, cognitive conflict and cortical brain activity
David W Evans, Patrick T Orr, Steven M Lazar, et al.
Human Molecular Genetics
|
May 16, 2009
Segmental duplications mediate novel, clinically relevant chromosome rearrangements
M Katharine Rudd, Julia Keene, Brian Bunke, et al.
Genomics
|
July 3, 2003
Complex low-copy repeats associated with a common polymorphic inversion at human chromosome 8p23
Hirobumi Sugawara, Naoki Harada, Tomoko Ida, et al.
JAMA Pediatrics
|
March 6, 2023
Diagnostic Yield of Exome Sequencing in Cerebral Palsy and Implications for Genetic Testing Guidelines: A Systematic Review and Meta-analysis
Pedro J Gonzalez-Mantilla, Yirui Hu, Scott M Myers, et al.
Page
of 13