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David H Ledbetter

Showing results (101-110 of 125) with videos related to

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Science (New York, N.Y.)|December 24, 2016
Genetic identification of familial hypercholesterolemia within a single U.S. health care systemNoura S Abul-Husn, Kandamurugu Manickam, Laney K Jones, et al.
Journal of Medical Genetics|October 12, 2012
A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disordersFlore Zufferey, Elliott H Sherr, Noam D Beckmann, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|March 18, 2014
Characterizing genetic variants for clinical actionErin M Ramos, Corina Din-Lovinescu, Jonathan S Berg, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 14, 2021
Correction to: Early cancer diagnoses through BRCA1/2 screening of unselected adult biobank participantsAdam H Buchanan, Kandamurugu Manickam, Michelle N Meyer, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 21, 2017
Early cancer diagnoses through BRCA1/2 screening of unselected adult biobank participantsAdam H Buchanan, Kandamurugu Manickam, Michelle N Meyer, et al.
Journal of the American College of Cardiology|August 4, 2018
Clinical Genetic Testing for Familial Hypercholesterolemia: JACC Scientific Expert PanelAmy C Sturm, Joshua W Knowles, Samuel S Gidding, et al.
American Journal of Human Genetics|May 15, 2010
Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomaliesDavid T Miller, Margaret P Adam, Swaroop Aradhya, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 17, 2011
An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilitiesErin B Kaminsky, Vineith Kaul, Justin Paschall, et al.
Frontiers in Genetics|September 2, 2014
Phenome-wide association studies demonstrating pleiotropy of genetic variants within FTO with and without adjustment for body mass indexRobert M Cronin, Julie R Field, Yuki Bradford, et al.
American Journal of Human Genetics|November 9, 2010
Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophreniaDaniel Moreno-De-Luca, , Jennifer G Mulle, et al.
Pageof 13

Showing results (101-110 of 125) with videos related to

Sort By:
Pageof 13
Science (New York, N.Y.)|December 24, 2016
Genetic identification of familial hypercholesterolemia within a single U.S. health care systemNoura S Abul-Husn, Kandamurugu Manickam, Laney K Jones, et al.
Journal of Medical Genetics|October 12, 2012
A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disordersFlore Zufferey, Elliott H Sherr, Noam D Beckmann, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|March 18, 2014
Characterizing genetic variants for clinical actionErin M Ramos, Corina Din-Lovinescu, Jonathan S Berg, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 14, 2021
Correction to: Early cancer diagnoses through BRCA1/2 screening of unselected adult biobank participantsAdam H Buchanan, Kandamurugu Manickam, Michelle N Meyer, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 21, 2017
Early cancer diagnoses through BRCA1/2 screening of unselected adult biobank participantsAdam H Buchanan, Kandamurugu Manickam, Michelle N Meyer, et al.
Journal of the American College of Cardiology|August 4, 2018
Clinical Genetic Testing for Familial Hypercholesterolemia: JACC Scientific Expert PanelAmy C Sturm, Joshua W Knowles, Samuel S Gidding, et al.
American Journal of Human Genetics|May 15, 2010
Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomaliesDavid T Miller, Margaret P Adam, Swaroop Aradhya, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 17, 2011
An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilitiesErin B Kaminsky, Vineith Kaul, Justin Paschall, et al.
Frontiers in Genetics|September 2, 2014
Phenome-wide association studies demonstrating pleiotropy of genetic variants within FTO with and without adjustment for body mass indexRobert M Cronin, Julie R Field, Yuki Bradford, et al.
American Journal of Human Genetics|November 9, 2010
Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophreniaDaniel Moreno-De-Luca, , Jennifer G Mulle, et al.
Pageof 13