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JACC. Advances
|
March 27, 2025
Polygenic Risk Scores in Myocardial Injury After Noncardiac Surgery: A VISION Substudy
Ann Le, Guillaume Paré, P J Devereaux, et al.
Trials
|
April 2, 2021
A clinical and cost-effectiveness trial of a parent group intervention to manage challenging restricted and repetitive behaviours in young children with autism spectrum disorder: study protocol for a randomised controlled trial
Victoria Grahame, Linda Dixon, Sue Fletcher-Watson, et al.
Human Genetics
|
October 15, 2011
A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder
Jillian P Casey, Tiago Magalhaes, Judith M Conroy, et al.
Nature Genetics
|
February 27, 2007
Mapping autism risk loci using genetic linkage and chromosomal rearrangements
, Peter Szatmari, Andrew D Paterson, et al.
Human Molecular Genetics
|
July 31, 2012
Individual common variants exert weak effects on the risk for autism spectrum disorders
Richard Anney, Lambertus Klei, Dalila Pinto, et al.
Human Molecular Genetics
|
July 29, 2010
A genome-wide scan for common alleles affecting risk for autism
Richard Anney, Lambertus Klei, Dalila Pinto, et al.
Nature
|
June 10, 2010
Functional impact of global rare copy number variation in autism spectrum disorders
Dalila Pinto, Alistair T Pagnamenta, Lambertus Klei, et al.
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Search research articles
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Showing results (101-110 of 107) with videos related to
Sort By:
Page
of 11
You have reached the last page of results.
This site can display upto 107 results.
JACC. Advances
|
March 27, 2025
Polygenic Risk Scores in Myocardial Injury After Noncardiac Surgery: A VISION Substudy
Ann Le, Guillaume Paré, P J Devereaux, et al.
Trials
|
April 2, 2021
A clinical and cost-effectiveness trial of a parent group intervention to manage challenging restricted and repetitive behaviours in young children with autism spectrum disorder: study protocol for a randomised controlled trial
Victoria Grahame, Linda Dixon, Sue Fletcher-Watson, et al.
Human Genetics
|
October 15, 2011
A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder
Jillian P Casey, Tiago Magalhaes, Judith M Conroy, et al.
Nature Genetics
|
February 27, 2007
Mapping autism risk loci using genetic linkage and chromosomal rearrangements
, Peter Szatmari, Andrew D Paterson, et al.
Human Molecular Genetics
|
July 31, 2012
Individual common variants exert weak effects on the risk for autism spectrum disorders
Richard Anney, Lambertus Klei, Dalila Pinto, et al.
Human Molecular Genetics
|
July 29, 2010
A genome-wide scan for common alleles affecting risk for autism
Richard Anney, Lambertus Klei, Dalila Pinto, et al.
Nature
|
June 10, 2010
Functional impact of global rare copy number variation in autism spectrum disorders
Dalila Pinto, Alistair T Pagnamenta, Lambertus Klei, et al.
Page
of 11