The Experts below are selected from a list of 309 Experts worldwide ranked by ideXlab platform
Fady M. Mikhail - One of the best experts on this subject based on the ideXlab platform.
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Clinical relevance of small copy-number variants in chromosomal microarray Clinical Testing
Genetics in Medicine, 2017Co-Authors: Dana Hollenbeck, Crescenda L. Williams, Kathryn T. Drazba, Maria Descartes, Bruce R. Korf, S. Lane Rutledge, Edward J. Lose, Nathaniel H. Robin, Andrew J. Carroll, Fady M. MikhailAbstract:Genet Med 19 4, 377–385. Purpose: The 2010 consensus statement on diagnostic chromosomal microarray (CMA) Testing recommended an array resolution ≥400 kb throughout the genome as a balance of analytical and Clinical sensitivity. In spite of the clear evidence for pathogenicity of large copy-number variants (CNVs) in neurodevelopmental disorders and/or congenital anomalies, the significance of small, nonrecurrent CNVs (
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Clinical relevance of small copy-number variants in chromosomal microarray Clinical Testing.
Genetics in Medicine, 2016Co-Authors: Dana Hollenbeck, Crescenda L. Williams, Kathryn T. Drazba, Maria Descartes, Bruce R. Korf, S. Lane Rutledge, Edward J. Lose, Nathaniel H. Robin, Andrew J. Carroll, Fady M. MikhailAbstract:Clinical relevance of small copy-number variants in chromosomal microarray Clinical Testing
Dana Hollenbeck - One of the best experts on this subject based on the ideXlab platform.
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Clinical relevance of small copy-number variants in chromosomal microarray Clinical Testing
Genetics in Medicine, 2017Co-Authors: Dana Hollenbeck, Crescenda L. Williams, Kathryn T. Drazba, Maria Descartes, Bruce R. Korf, S. Lane Rutledge, Edward J. Lose, Nathaniel H. Robin, Andrew J. Carroll, Fady M. MikhailAbstract:Genet Med 19 4, 377–385. Purpose: The 2010 consensus statement on diagnostic chromosomal microarray (CMA) Testing recommended an array resolution ≥400 kb throughout the genome as a balance of analytical and Clinical sensitivity. In spite of the clear evidence for pathogenicity of large copy-number variants (CNVs) in neurodevelopmental disorders and/or congenital anomalies, the significance of small, nonrecurrent CNVs (
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Clinical relevance of small copy-number variants in chromosomal microarray Clinical Testing.
Genetics in Medicine, 2016Co-Authors: Dana Hollenbeck, Crescenda L. Williams, Kathryn T. Drazba, Maria Descartes, Bruce R. Korf, S. Lane Rutledge, Edward J. Lose, Nathaniel H. Robin, Andrew J. Carroll, Fady M. MikhailAbstract:Clinical relevance of small copy-number variants in chromosomal microarray Clinical Testing
Maria Descartes - One of the best experts on this subject based on the ideXlab platform.
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Clinical relevance of small copy-number variants in chromosomal microarray Clinical Testing
Genetics in Medicine, 2017Co-Authors: Dana Hollenbeck, Crescenda L. Williams, Kathryn T. Drazba, Maria Descartes, Bruce R. Korf, S. Lane Rutledge, Edward J. Lose, Nathaniel H. Robin, Andrew J. Carroll, Fady M. MikhailAbstract:Genet Med 19 4, 377–385. Purpose: The 2010 consensus statement on diagnostic chromosomal microarray (CMA) Testing recommended an array resolution ≥400 kb throughout the genome as a balance of analytical and Clinical sensitivity. In spite of the clear evidence for pathogenicity of large copy-number variants (CNVs) in neurodevelopmental disorders and/or congenital anomalies, the significance of small, nonrecurrent CNVs (
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Clinical relevance of small copy-number variants in chromosomal microarray Clinical Testing.
Genetics in Medicine, 2016Co-Authors: Dana Hollenbeck, Crescenda L. Williams, Kathryn T. Drazba, Maria Descartes, Bruce R. Korf, S. Lane Rutledge, Edward J. Lose, Nathaniel H. Robin, Andrew J. Carroll, Fady M. MikhailAbstract:Clinical relevance of small copy-number variants in chromosomal microarray Clinical Testing
Crescenda L. Williams - One of the best experts on this subject based on the ideXlab platform.
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Clinical relevance of small copy-number variants in chromosomal microarray Clinical Testing
Genetics in Medicine, 2017Co-Authors: Dana Hollenbeck, Crescenda L. Williams, Kathryn T. Drazba, Maria Descartes, Bruce R. Korf, S. Lane Rutledge, Edward J. Lose, Nathaniel H. Robin, Andrew J. Carroll, Fady M. MikhailAbstract:Genet Med 19 4, 377–385. Purpose: The 2010 consensus statement on diagnostic chromosomal microarray (CMA) Testing recommended an array resolution ≥400 kb throughout the genome as a balance of analytical and Clinical sensitivity. In spite of the clear evidence for pathogenicity of large copy-number variants (CNVs) in neurodevelopmental disorders and/or congenital anomalies, the significance of small, nonrecurrent CNVs (
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Clinical relevance of small copy-number variants in chromosomal microarray Clinical Testing.
Genetics in Medicine, 2016Co-Authors: Dana Hollenbeck, Crescenda L. Williams, Kathryn T. Drazba, Maria Descartes, Bruce R. Korf, S. Lane Rutledge, Edward J. Lose, Nathaniel H. Robin, Andrew J. Carroll, Fady M. MikhailAbstract:Clinical relevance of small copy-number variants in chromosomal microarray Clinical Testing
Bruce R. Korf - One of the best experts on this subject based on the ideXlab platform.
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Clinical relevance of small copy-number variants in chromosomal microarray Clinical Testing
Genetics in Medicine, 2017Co-Authors: Dana Hollenbeck, Crescenda L. Williams, Kathryn T. Drazba, Maria Descartes, Bruce R. Korf, S. Lane Rutledge, Edward J. Lose, Nathaniel H. Robin, Andrew J. Carroll, Fady M. MikhailAbstract:Genet Med 19 4, 377–385. Purpose: The 2010 consensus statement on diagnostic chromosomal microarray (CMA) Testing recommended an array resolution ≥400 kb throughout the genome as a balance of analytical and Clinical sensitivity. In spite of the clear evidence for pathogenicity of large copy-number variants (CNVs) in neurodevelopmental disorders and/or congenital anomalies, the significance of small, nonrecurrent CNVs (
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Clinical relevance of small copy-number variants in chromosomal microarray Clinical Testing.
Genetics in Medicine, 2016Co-Authors: Dana Hollenbeck, Crescenda L. Williams, Kathryn T. Drazba, Maria Descartes, Bruce R. Korf, S. Lane Rutledge, Edward J. Lose, Nathaniel H. Robin, Andrew J. Carroll, Fady M. MikhailAbstract:Clinical relevance of small copy-number variants in chromosomal microarray Clinical Testing