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Showing results (1321-1330 of 1,361) with videos related to
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JAMA
|
November 6, 2007
Implementation of a statewide system for coronary reperfusion for ST-segment elevation myocardial infarction
James G Jollis, Mayme L Roettig, Akinyele O Aluko, et al.
European Journal of Human Genetics : EJHG
|
January 21, 2010
Association between genes on chromosome 4p16 and non-syndromic oral clefts in four populations
Roxann G Ingersoll, Jacqueline Hetmanski, Ji-Wan Park, et al.
Genetics
|
May 6, 2014
Whole exome sequencing of distant relatives in multiplex families implicates rare variants in candidate genes for oral clefts
Alexandre Bureau, Margaret M Parker, Ingo Ruczinski, et al.
American Journal of Medical Genetics. Part A
|
March 16, 2012
Genome wide study of maternal and parent-of-origin effects on the etiology of orofacial clefts
Min Shi, Jeffrey C Murray, Mary L Marazita, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
April 29, 2016
A standardized, evidence-based protocol to assess clinical actionability of genetic disorders associated with genomic variation
Jessica Ezzell Hunter, Stephanie A Irving, Leslie G Biesecker, et al.
Biorxiv : the Preprint Server for Biology
|
December 9, 2024
Folate prevents the autism-related phenotype caused by developmental pyrethroid exposure in prairie voles
Nilanjana Saferin, Ibrahim Haseeb, Adam M Taha, et al.
Critical Care Medicine
|
October 6, 2021
Criteria for Pediatric Sepsis-A Systematic Review and Meta-Analysis by the Pediatric Sepsis Definition Taskforce
Kusum Menon, Luregn J Schlapbach, Samuel Akech, et al.
Cell Death & Disease
|
December 20, 2025
Targeting secreted PLA<sub>2</sub> interactions with EGFR and vimentin to arrest prostate tumour growth
Timothy J Mann, Ryung Rae Kim, Mila Sajinovic, et al.
American Journal of Human Genetics
|
May 30, 2017
Evaluating the Clinical Validity of Gene-Disease Associations: An Evidence-Based Framework Developed by the Clinical Genome Resource
Natasha T Strande, Erin Rooney Riggs, Adam H Buchanan, et al.
Nature Genetics
|
October 2, 2012
Mutations in the TGF-β repressor SKI cause Shprintzen-Goldberg syndrome with aortic aneurysm
Alexander J Doyle, Jefferson J Doyle, Seneca L Bessling, et al.
Page
of 137
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Showing results (1321-1330 of 1,361) with videos related to
Sort By:
Page
of 137
JAMA
|
November 6, 2007
Implementation of a statewide system for coronary reperfusion for ST-segment elevation myocardial infarction
James G Jollis, Mayme L Roettig, Akinyele O Aluko, et al.
European Journal of Human Genetics : EJHG
|
January 21, 2010
Association between genes on chromosome 4p16 and non-syndromic oral clefts in four populations
Roxann G Ingersoll, Jacqueline Hetmanski, Ji-Wan Park, et al.
Genetics
|
May 6, 2014
Whole exome sequencing of distant relatives in multiplex families implicates rare variants in candidate genes for oral clefts
Alexandre Bureau, Margaret M Parker, Ingo Ruczinski, et al.
American Journal of Medical Genetics. Part A
|
March 16, 2012
Genome wide study of maternal and parent-of-origin effects on the etiology of orofacial clefts
Min Shi, Jeffrey C Murray, Mary L Marazita, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
April 29, 2016
A standardized, evidence-based protocol to assess clinical actionability of genetic disorders associated with genomic variation
Jessica Ezzell Hunter, Stephanie A Irving, Leslie G Biesecker, et al.
Biorxiv : the Preprint Server for Biology
|
December 9, 2024
Folate prevents the autism-related phenotype caused by developmental pyrethroid exposure in prairie voles
Nilanjana Saferin, Ibrahim Haseeb, Adam M Taha, et al.
Critical Care Medicine
|
October 6, 2021
Criteria for Pediatric Sepsis-A Systematic Review and Meta-Analysis by the Pediatric Sepsis Definition Taskforce
Kusum Menon, Luregn J Schlapbach, Samuel Akech, et al.
Cell Death & Disease
|
December 20, 2025
Targeting secreted PLA<sub>2</sub> interactions with EGFR and vimentin to arrest prostate tumour growth
Timothy J Mann, Ryung Rae Kim, Mila Sajinovic, et al.
American Journal of Human Genetics
|
May 30, 2017
Evaluating the Clinical Validity of Gene-Disease Associations: An Evidence-Based Framework Developed by the Clinical Genome Resource
Natasha T Strande, Erin Rooney Riggs, Adam H Buchanan, et al.
Nature Genetics
|
October 2, 2012
Mutations in the TGF-β repressor SKI cause Shprintzen-Goldberg syndrome with aortic aneurysm
Alexander J Doyle, Jefferson J Doyle, Seneca L Bessling, et al.
Page
of 137