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Pharmacoepidemiology and Drug Safety
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May 15, 2026
Atypical Shoulder Pain and Dysfunction After Vaccinations Reported to the Vaccine Adverse Event Reporting System (VAERS) January 1, 2018, Through October 31, 2022
Elaine R Miller, Paige Marquez, Getahun Aynalem, et al.
Medrxiv : the Preprint Server for Health Sciences
|
May 15, 2024
Genome Sequencing is Critical for Forecasting Outcomes Following Congenital Cardiac Surgery
W Scott Watkins, E Javier Hernandez, Thomas Miller, et al.
Orphanet Journal of Rare Diseases
|
November 15, 2013
Clinical characteristics of patients with spinocerebellar ataxias 1, 2, 3 and 6 in the US; a prospective observational study
Tetsuo Ashizawa, Karla P Figueroa, Susan L Perlman, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 13, 2018
A gene-centric strategy for identifying disease-causing rare variants in dilated cardiomyopathy
Claire Horvat, Renee Johnson, Lien Lam, et al.
American Journal of Medical Genetics. Part A
|
April 23, 2015
The third international meeting on genetic disorders in the RAS/MAPK pathway: towards a therapeutic approach
Bruce Korf, Reza Ahmadian, Judith Allanson, et al.
American Journal of Medical Genetics. Part A
|
May 8, 2016
The Fourth International Symposium on Genetic Disorders of the Ras/MAPK pathway
David A Stevenson, Lisa Schill, Lisa Schoyer, et al.
American Journal of Medical Genetics. Part A
|
January 5, 2011
Genotype-phenotype analysis of the branchio-oculo-facial syndrome
Jeff M Milunsky, Tom M Maher, Geping Zhao, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 13, 2016
Recommendations for the integration of genomics into clinical practice
Sarah Bowdin, Adel Gilbert, Emma Bedoukian, et al.
American Journal of Medical Genetics. Part A
|
December 12, 2019
The sixth international RASopathies symposium: Precision medicine-From promise to practice
Karen W Gripp, Lisa Schill, Lisa Schoyer, et al.
HGG Advances
|
February 20, 2026
Scaling Genomic Reanalysis to Unlock Diagnoses and Transform Rare Disease Care
Shira Rockowitz, Wanqing Shao, Courtney French, et al.
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of 5
Search research articles
Search
Showing results (31-40 of 47) with videos related to
Sort By:
Page
of 5
Pharmacoepidemiology and Drug Safety
|
May 15, 2026
Atypical Shoulder Pain and Dysfunction After Vaccinations Reported to the Vaccine Adverse Event Reporting System (VAERS) January 1, 2018, Through October 31, 2022
Elaine R Miller, Paige Marquez, Getahun Aynalem, et al.
Medrxiv : the Preprint Server for Health Sciences
|
May 15, 2024
Genome Sequencing is Critical for Forecasting Outcomes Following Congenital Cardiac Surgery
W Scott Watkins, E Javier Hernandez, Thomas Miller, et al.
Orphanet Journal of Rare Diseases
|
November 15, 2013
Clinical characteristics of patients with spinocerebellar ataxias 1, 2, 3 and 6 in the US; a prospective observational study
Tetsuo Ashizawa, Karla P Figueroa, Susan L Perlman, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 13, 2018
A gene-centric strategy for identifying disease-causing rare variants in dilated cardiomyopathy
Claire Horvat, Renee Johnson, Lien Lam, et al.
American Journal of Medical Genetics. Part A
|
April 23, 2015
The third international meeting on genetic disorders in the RAS/MAPK pathway: towards a therapeutic approach
Bruce Korf, Reza Ahmadian, Judith Allanson, et al.
American Journal of Medical Genetics. Part A
|
May 8, 2016
The Fourth International Symposium on Genetic Disorders of the Ras/MAPK pathway
David A Stevenson, Lisa Schill, Lisa Schoyer, et al.
American Journal of Medical Genetics. Part A
|
January 5, 2011
Genotype-phenotype analysis of the branchio-oculo-facial syndrome
Jeff M Milunsky, Tom M Maher, Geping Zhao, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 13, 2016
Recommendations for the integration of genomics into clinical practice
Sarah Bowdin, Adel Gilbert, Emma Bedoukian, et al.
American Journal of Medical Genetics. Part A
|
December 12, 2019
The sixth international RASopathies symposium: Precision medicine-From promise to practice
Karen W Gripp, Lisa Schill, Lisa Schoyer, et al.
HGG Advances
|
February 20, 2026
Scaling Genomic Reanalysis to Unlock Diagnoses and Transform Rare Disease Care
Shira Rockowitz, Wanqing Shao, Courtney French, et al.
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of 5