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Showing results (361-370 of 388) with videos related to

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The American Journal of Psychiatry|March 3, 2022
Genes To Mental Health (G2MH): A Framework to Map the Combined Effects of Rare and Common Variants on Dimensions of Cognition and PsychopathologySébastien Jacquemont, Guillaume Huguet, Marieke Klein, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 5, 2017
Electronic health record phenotype in subjects with genetic variants associated with arrhythmogenic right ventricular cardiomyopathy: a study of 30,716 subjects with exome sequencingChristopher M Haggerty, Cynthia A James, Hugh Calkins, et al.
Brain : a Journal of Neurology|October 23, 2002
Subcortical band heterotopia (SBH) in males: clinical, imaging and genetic findings in comparison with femalesMaria Daniela D'Agostino, Andrea Bernasconi, Soma Das, et al.
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.
Pageof 39

Showing results (361-370 of 388) with videos related to

Sort By:
Pageof 39
The American Journal of Psychiatry|March 3, 2022
Genes To Mental Health (G2MH): A Framework to Map the Combined Effects of Rare and Common Variants on Dimensions of Cognition and PsychopathologySébastien Jacquemont, Guillaume Huguet, Marieke Klein, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 5, 2017
Electronic health record phenotype in subjects with genetic variants associated with arrhythmogenic right ventricular cardiomyopathy: a study of 30,716 subjects with exome sequencingChristopher M Haggerty, Cynthia A James, Hugh Calkins, et al.
Brain : a Journal of Neurology|October 23, 2002
Subcortical band heterotopia (SBH) in males: clinical, imaging and genetic findings in comparison with femalesMaria Daniela D'Agostino, Andrea Bernasconi, Soma Das, et al.
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.
Pageof 39