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

N Van Der Aa

Showing results (1-10 of 10) with videos related to

Pageof 1
Sort By:
JBR-BTR : Organe De La Societe Royale Belge De Radiologie (SRBR) = Orgaan Van De Koninklijke Belgische Vereniging Voor Radiologie (KBVR)|April 11, 2009
The French telephone receiver sign in thanatophoric dysplasiaF M Vanhoenacker, N Van der Aa, B Blaumeiser
The Journal of Pediatrics|January 15, 1998
Respiratory syncytial virus bronchiolitis: a double-blind dexamethasone efficacy studyK De Boeck, N Van der Aa, S Van Lierde, et al.
Pediatric Pulmonology|July 15, 2009
'Difficult asthma': can symptoms be controlled in a structured environment?K De Boeck, M Moens, N Van Der Aa, et al.
Molecular Syndromology|December 23, 2011
Analysis of FOXG1 Is Highly Recommended in Male and Female Patients with Rett SyndromeN Van der Aa, M Van den Bergh, N Ponomarenko, et al.
Clinical Genetics|August 2, 2014
Challenges and opportunities in the investigation of unexplained intellectual disability using family-based whole-exome sequencingC Helsmoortel, G Vandeweyer, P Ordoukhanian, et al.
The Journal of Urology|February 2, 2013
Hypermethylation of the polycomb group target gene PCDH7 in bladder tumors from patients of all agesWillemien Beukers, Aleksander Hercegovac, Marcel Vermeij, et al.
Acta Anaesthesiologica Scandinavica|January 21, 2012
Inborn oxidative phosphorylation defect as risk factor for propofol infusion syndromeA V Vanlander, P G Jorens, J Smet, et al.
Molecular Syndromology|May 9, 2013
Evaluation of Clinical Manifestations in Patients with Severe Lymphedema with and without CCBE1 MutationsM Alders, A Mendola, L Adès, et al.
Journal of Medical Genetics|July 17, 2008
Clinical and molecular delineation of the 17q21.31 microdeletion syndromeD A Koolen, A J Sharp, J A Hurst, et al.
Journal of Medical Genetics|April 18, 2009
Further delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a severe outcomeB W M van Bon, H C Mefford, B Menten, et al.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
JBR-BTR : Organe De La Societe Royale Belge De Radiologie (SRBR) = Orgaan Van De Koninklijke Belgische Vereniging Voor Radiologie (KBVR)|April 11, 2009
The French telephone receiver sign in thanatophoric dysplasiaF M Vanhoenacker, N Van der Aa, B Blaumeiser
The Journal of Pediatrics|January 15, 1998
Respiratory syncytial virus bronchiolitis: a double-blind dexamethasone efficacy studyK De Boeck, N Van der Aa, S Van Lierde, et al.
Pediatric Pulmonology|July 15, 2009
'Difficult asthma': can symptoms be controlled in a structured environment?K De Boeck, M Moens, N Van Der Aa, et al.
Molecular Syndromology|December 23, 2011
Analysis of FOXG1 Is Highly Recommended in Male and Female Patients with Rett SyndromeN Van der Aa, M Van den Bergh, N Ponomarenko, et al.
Clinical Genetics|August 2, 2014
Challenges and opportunities in the investigation of unexplained intellectual disability using family-based whole-exome sequencingC Helsmoortel, G Vandeweyer, P Ordoukhanian, et al.
The Journal of Urology|February 2, 2013
Hypermethylation of the polycomb group target gene PCDH7 in bladder tumors from patients of all agesWillemien Beukers, Aleksander Hercegovac, Marcel Vermeij, et al.
Acta Anaesthesiologica Scandinavica|January 21, 2012
Inborn oxidative phosphorylation defect as risk factor for propofol infusion syndromeA V Vanlander, P G Jorens, J Smet, et al.
Molecular Syndromology|May 9, 2013
Evaluation of Clinical Manifestations in Patients with Severe Lymphedema with and without CCBE1 MutationsM Alders, A Mendola, L Adès, et al.
Journal of Medical Genetics|July 17, 2008
Clinical and molecular delineation of the 17q21.31 microdeletion syndromeD A Koolen, A J Sharp, J A Hurst, et al.
Journal of Medical Genetics|April 18, 2009
Further delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a severe outcomeB W M van Bon, H C Mefford, B Menten, et al.
Pageof 1