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

A Bonnard

Showing results (41-50 of 44) with videos related to

Pageof 5
Sort By:
You have reached the last page of results.This site can display upto 44 results.
Acta Paediatrica (Oslo, Norway : 1992)|July 3, 2013
Paediatric and adolescent traumatic gastrointestinal injuries: results of a European multicentre analysisE E Fischerauer, S Zötsch, C Capito, et al.
Haematologica|November 20, 2023
Germline bi-allelic <i>SH2B3/LNK</i> alteration predisposes to a neonatal juvenile myelomonocytic leukemia-like disorderChloé Arfeuille, Yoann Vial, Margaux Cadenet, et al.
Human Molecular Genetics|March 29, 2022
Expanding the molecular spectrum of pathogenic SHOC2 variants underlying Mazzanti syndromeMarialetizia Motta, Maja Solman, Adeline A Bonnard, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|January 22, 2015
[Does prenatal diagnosis modify neonatal management and early outcome of children with esophageal atresia type III?]C Garabedian, R Sfeir, C Langlois, et al.
Pageof 5

Showing results (41-50 of 44) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 44 results.
Acta Paediatrica (Oslo, Norway : 1992)|July 3, 2013
Paediatric and adolescent traumatic gastrointestinal injuries: results of a European multicentre analysisE E Fischerauer, S Zötsch, C Capito, et al.
Haematologica|November 20, 2023
Germline bi-allelic <i>SH2B3/LNK</i> alteration predisposes to a neonatal juvenile myelomonocytic leukemia-like disorderChloé Arfeuille, Yoann Vial, Margaux Cadenet, et al.
Human Molecular Genetics|March 29, 2022
Expanding the molecular spectrum of pathogenic SHOC2 variants underlying Mazzanti syndromeMarialetizia Motta, Maja Solman, Adeline A Bonnard, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|January 22, 2015
[Does prenatal diagnosis modify neonatal management and early outcome of children with esophageal atresia type III?]C Garabedian, R Sfeir, C Langlois, et al.
Pageof 5