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K FitzGerald

Showing results (141-150 of 149) with videos related to

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Journal of Genetic Counseling|September 12, 2021
Genetic counseling for congenital heart disease - Practice resource of the National Society of Genetic CounselorsHannah E Ison, Emily L Griffin, Ashley Parrott, et al.
Journal of Thrombosis and Haemostasis : JTH|March 7, 2022
Effects of ex vivo blood anticoagulation and preanalytical processing time on the proteome content of plateletsSamuel Tassi Yunga, Austin J Gower, Alexander R Melrose, et al.
Journal of Dental Research|December 16, 2017
Hypercementosis Associated with ENPP1 Mutations and GACIV Thumbigere-Math, A Alqadi, N I Chalmers, et al.
Pediatrics|August 3, 2001
Growth and development in preterm infants fed long-chain polyunsaturated fatty acids: a prospective, randomized controlled trialD L O'Connor, R Hall, D Adamkin, et al.
JAMA Cardiology|January 9, 2020
Identification of a Novel Homozygous Multi-Exon Duplication in RYR2 Among Children With Exertion-Related Unexplained Sudden Deaths in the Amish CommunityDavid J Tester, Hannah M Bombei, Kristi K Fitzgerald, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|August 2, 2019
The genetic diversity of multiple sclerosis risk among Hispanic and African American populations living in the United StatesA H Beecham, L Amezcua, A Chinea, et al.
Microbiology Resource Announcements|March 12, 2021
Genome Sequences of Subcluster M2 Mycobacteriophages Estes and AzizSara K Fitzgerald, Eleanor H Johnson, Sophie H R Storz, et al.
American Journal of Human Genetics|June 21, 2008
Infantile spasms is associated with deletion of the MAGI2 gene on chromosome 7q11.23-q21.11Christian R Marshall, Edwin J Young, Ariel M Pani, et al.
American Journal of Human Genetics|January 11, 2025
DNA-binding affinity and specificity determine the phenotypic diversity in BCL11B-related disordersIvana Lessel, Anja Baresic, Ivan K Chinn, et al.
Pageof 15

Showing results (141-150 of 149) with videos related to

Sort By:
Pageof 15
You have reached the last page of results.This site can display upto 149 results.
Journal of Genetic Counseling|September 12, 2021
Genetic counseling for congenital heart disease - Practice resource of the National Society of Genetic CounselorsHannah E Ison, Emily L Griffin, Ashley Parrott, et al.
Journal of Thrombosis and Haemostasis : JTH|March 7, 2022
Effects of ex vivo blood anticoagulation and preanalytical processing time on the proteome content of plateletsSamuel Tassi Yunga, Austin J Gower, Alexander R Melrose, et al.
Journal of Dental Research|December 16, 2017
Hypercementosis Associated with ENPP1 Mutations and GACIV Thumbigere-Math, A Alqadi, N I Chalmers, et al.
Pediatrics|August 3, 2001
Growth and development in preterm infants fed long-chain polyunsaturated fatty acids: a prospective, randomized controlled trialD L O'Connor, R Hall, D Adamkin, et al.
JAMA Cardiology|January 9, 2020
Identification of a Novel Homozygous Multi-Exon Duplication in RYR2 Among Children With Exertion-Related Unexplained Sudden Deaths in the Amish CommunityDavid J Tester, Hannah M Bombei, Kristi K Fitzgerald, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|August 2, 2019
The genetic diversity of multiple sclerosis risk among Hispanic and African American populations living in the United StatesA H Beecham, L Amezcua, A Chinea, et al.
Microbiology Resource Announcements|March 12, 2021
Genome Sequences of Subcluster M2 Mycobacteriophages Estes and AzizSara K Fitzgerald, Eleanor H Johnson, Sophie H R Storz, et al.
American Journal of Human Genetics|June 21, 2008
Infantile spasms is associated with deletion of the MAGI2 gene on chromosome 7q11.23-q21.11Christian R Marshall, Edwin J Young, Ariel M Pani, et al.
American Journal of Human Genetics|January 11, 2025
DNA-binding affinity and specificity determine the phenotypic diversity in BCL11B-related disordersIvana Lessel, Anja Baresic, Ivan K Chinn, et al.
Pageof 15