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Science (New York, N.Y.)
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December 24, 2016
Genetic identification of familial hypercholesterolemia within a single U.S. health care system
Noura 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 disorders
Flore 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 action
Erin 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 participants
Adam 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 participants
Adam 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 Panel
Amy 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 anomalies
David 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 disabilities
Erin 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 index
Robert 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 schizophrenia
Daniel Moreno-De-Luca, , Jennifer G Mulle, et al.
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Search research articles
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Showing results (101-110 of 125) with videos related to
Sort By:
Page
of 13
Science (New York, N.Y.)
|
December 24, 2016
Genetic identification of familial hypercholesterolemia within a single U.S. health care system
Noura 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 disorders
Flore 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 action
Erin 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 participants
Adam 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 participants
Adam 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 Panel
Amy 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 anomalies
David 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 disabilities
Erin 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 index
Robert 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 schizophrenia
Daniel Moreno-De-Luca, , Jennifer G Mulle, et al.
Page
of 13