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

L Marcelis

Showing results (31-40 of 46) with videos related to

Pageof 5
Sort By:
European Journal of Cancer (Oxford, England : 1990)|May 28, 2024
Neoadjuvant immunotherapy in microsatellite instability-high (MSI-H) duodenal adenocarcinoma leads to pathological complete response and paves the way for new strategiesS Ziane Bouziane, L Mans, A-M Bucalau, et al.
European Journal of Pediatrics|November 21, 2024
Four-year evaluation of neonatal cystic fibrosis screening in Southern BelgiumM Thimmesch, S Berardis, L Hanssens, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 30, 2010
Complete COL1A1 allele deletions in osteogenesis imperfectaFleur S van Dijk, Margriet Huizer, Ariana Kariminejad, et al.
American Journal of Medical Genetics. Part A|September 24, 2017
The spectrum of DNMT3A variants in Tatton-Brown-Rahman syndrome overlaps with that in hematologic malignanciesWei Shen, Jennifer M Heeley, Colleen M Carlston, et al.
Clinical Genetics|February 8, 2011
Intragenic deletion in DYRK1A leads to mental retardation and primary microcephalyB W M van Bon, A Hoischen, J Hehir-Kwa, et al.
American Journal of Medical Genetics. Part A|March 29, 2014
Early presentation of cystic kidneys in a family with a homozygous INVS mutationMachteld M Oud, Bregje W van Bon, Ernie M H F Bongers, et al.
Science (New York, N.Y.)|June 3, 2017
Neurodevelopmental protein Musashi-1 interacts with the Zika genome and promotes viral replicationPavithra L Chavali, Lovorka Stojic, Luke W Meredith, et al.
Annals of Neurology|July 18, 2018
Haploinsufficiency of CUX1 Causes Nonsyndromic Global Developmental Delay With Possible Catch-up DevelopmentKonrad Platzer, Benjamin Cogné, Jennifer Hague, et al.
European Journal of Human Genetics : EJHG|June 25, 2009
CRTAP mutations in lethal and severe osteogenesis imperfecta: the importance of combining biochemical and molecular genetic analysisFleur S Van Dijk, Isabel M Nesbitt, Peter G J Nikkels, et al.
Nature Genetics|February 18, 2014
A SWI/SNF-related autism syndrome caused by de novo mutations in ADNPCéline Helsmoortel, Anneke T Vulto-van Silfhout, Bradley P Coe, et al.
Pageof 5

Showing results (31-40 of 46) with videos related to

Sort By:
Pageof 5
European Journal of Cancer (Oxford, England : 1990)|May 28, 2024
Neoadjuvant immunotherapy in microsatellite instability-high (MSI-H) duodenal adenocarcinoma leads to pathological complete response and paves the way for new strategiesS Ziane Bouziane, L Mans, A-M Bucalau, et al.
European Journal of Pediatrics|November 21, 2024
Four-year evaluation of neonatal cystic fibrosis screening in Southern BelgiumM Thimmesch, S Berardis, L Hanssens, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 30, 2010
Complete COL1A1 allele deletions in osteogenesis imperfectaFleur S van Dijk, Margriet Huizer, Ariana Kariminejad, et al.
American Journal of Medical Genetics. Part A|September 24, 2017
The spectrum of DNMT3A variants in Tatton-Brown-Rahman syndrome overlaps with that in hematologic malignanciesWei Shen, Jennifer M Heeley, Colleen M Carlston, et al.
Clinical Genetics|February 8, 2011
Intragenic deletion in DYRK1A leads to mental retardation and primary microcephalyB W M van Bon, A Hoischen, J Hehir-Kwa, et al.
American Journal of Medical Genetics. Part A|March 29, 2014
Early presentation of cystic kidneys in a family with a homozygous INVS mutationMachteld M Oud, Bregje W van Bon, Ernie M H F Bongers, et al.
Science (New York, N.Y.)|June 3, 2017
Neurodevelopmental protein Musashi-1 interacts with the Zika genome and promotes viral replicationPavithra L Chavali, Lovorka Stojic, Luke W Meredith, et al.
Annals of Neurology|July 18, 2018
Haploinsufficiency of CUX1 Causes Nonsyndromic Global Developmental Delay With Possible Catch-up DevelopmentKonrad Platzer, Benjamin Cogné, Jennifer Hague, et al.
European Journal of Human Genetics : EJHG|June 25, 2009
CRTAP mutations in lethal and severe osteogenesis imperfecta: the importance of combining biochemical and molecular genetic analysisFleur S Van Dijk, Isabel M Nesbitt, Peter G J Nikkels, et al.
Nature Genetics|February 18, 2014
A SWI/SNF-related autism syndrome caused by de novo mutations in ADNPCéline Helsmoortel, Anneke T Vulto-van Silfhout, Bradley P Coe, et al.
Pageof 5