Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Meryl Altree

Showing results (11-20 of 17) with videos related to

Pageof 2
Sort By:
You have reached the last page of results.This site can display upto 17 results.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|October 10, 2008
Methionine-dependence phenotype in the de novo pathway in BRCA1 and BRCA2 mutation carriers with and without breast cancerSasja Beetstra, Graeme Suthers, Varinderpal Dhillon, et al.
Journal of Surgical Education|January 14, 2014
Laparoscopic skills maintenance: a randomized trial of virtual reality and box trainer simulatorsMontaha W Khan, Diwei Lin, Nicholas Marlow, et al.
American Journal of Medical Genetics|February 13, 2002
Study of 250 children with idiopathic mental retardation reveals nine cryptic and diverse subtelomeric chromosome anomaliesElizabeth Baker, Lyn Hinton, David F Callen, et al.
World Journal of Surgery|September 10, 2025
A Simple Solution for a Complex Problem: The "Sterile Cockpit" to Improve Ward RoundsEllie Treloar, Matheesha Herath, Meryl Altree, et al.
Blood|December 30, 2015
Novel germ line DDX41 mutations define families with a lower age of MDS/AML onset and lymphoid malignanciesMaya Lewinsohn, Anna L Brown, Luke M Weinel, et al.
Nature Genetics|September 6, 2011
Heritable GATA2 mutations associated with familial myelodysplastic syndrome and acute myeloid leukemiaChristopher N Hahn, Chan-Eng Chong, Catherine L Carmichael, et al.
Blood Advances|March 26, 2020
RUNX1-mutated families show phenotype heterogeneity and a somatic mutation profile unique to germline predisposed AMLAnna L Brown, Peer Arts, Catherine L Carmichael, et al.
Pageof 2

Showing results (11-20 of 17) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 17 results.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|October 10, 2008
Methionine-dependence phenotype in the de novo pathway in BRCA1 and BRCA2 mutation carriers with and without breast cancerSasja Beetstra, Graeme Suthers, Varinderpal Dhillon, et al.
Journal of Surgical Education|January 14, 2014
Laparoscopic skills maintenance: a randomized trial of virtual reality and box trainer simulatorsMontaha W Khan, Diwei Lin, Nicholas Marlow, et al.
American Journal of Medical Genetics|February 13, 2002
Study of 250 children with idiopathic mental retardation reveals nine cryptic and diverse subtelomeric chromosome anomaliesElizabeth Baker, Lyn Hinton, David F Callen, et al.
World Journal of Surgery|September 10, 2025
A Simple Solution for a Complex Problem: The "Sterile Cockpit" to Improve Ward RoundsEllie Treloar, Matheesha Herath, Meryl Altree, et al.
Blood|December 30, 2015
Novel germ line DDX41 mutations define families with a lower age of MDS/AML onset and lymphoid malignanciesMaya Lewinsohn, Anna L Brown, Luke M Weinel, et al.
Nature Genetics|September 6, 2011
Heritable GATA2 mutations associated with familial myelodysplastic syndrome and acute myeloid leukemiaChristopher N Hahn, Chan-Eng Chong, Catherine L Carmichael, et al.
Blood Advances|March 26, 2020
RUNX1-mutated families show phenotype heterogeneity and a somatic mutation profile unique to germline predisposed AMLAnna L Brown, Peer Arts, Catherine L Carmichael, et al.
Pageof 2