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C W Ockeloen

Showing results (1-10 of 9) with videos related to

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Nederlands Tijdschrift Voor Tandheelkunde|October 10, 2014
[Solitary median maxillary central incisor syndrome]E Scholtes, T Kawamoto, C W Ockeloen, et al.
Nederlands Tijdschrift Voor Tandheelkunde|June 3, 2014
[Tooth eruption disturbances and syndromes]B C M Oosterkamp, C W Ockeloen, C E L Carels, et al.
Human Genetics|October 5, 2016
Tooth agenesis and orofacial clefting: genetic brothers in arms?M Phan, F Conte, K D Khandelwal, et al.
Hormone Research in Paediatrics|April 3, 2015
Short Stature in KBG Syndrome: First Responses to Growth Hormone TreatmentNele Reynaert, C W Ockeloen, L Sävendahl, et al.
Clinical Genetics|April 6, 2013
Novel BCOR mutations in patients with oculofaciocardiodental (OFCD) syndromeH E Feberwee, I Feenstra, S Oberoi, et al.
Human Genetics|August 13, 2015
'Splitting versus lumping': Temple-Baraitser and Zimmermann-Laband SyndromesNuria C Bramswig, C W Ockeloen, J C Czeschik, et al.
Neuromuscular Disorders : NMD|May 8, 2012
Congenital myopathy caused by a novel missense mutation in the CFL2 geneC W Ockeloen, H J Gilhuis, R Pfundt, et al.
American Journal of Medical Genetics. Part A|June 24, 2025
An International ASXL3 Natural History Study: Deep Phenotypic Analyses Including Detailed Reports of a Milder Phenotype, Novel Associations, and Clinical RecommendationsE Woods, N Holmes, A S Denommé-Pichon, et al.
Molecular Syndromology|December 6, 2011
Sixteen New Cases Contributing to the Characterization of Patients with Distal 22q11.2 MicroduplicationsJ Wincent, D L Bruno, B W M van Bon, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Nederlands Tijdschrift Voor Tandheelkunde|October 10, 2014
[Solitary median maxillary central incisor syndrome]E Scholtes, T Kawamoto, C W Ockeloen, et al.
Nederlands Tijdschrift Voor Tandheelkunde|June 3, 2014
[Tooth eruption disturbances and syndromes]B C M Oosterkamp, C W Ockeloen, C E L Carels, et al.
Human Genetics|October 5, 2016
Tooth agenesis and orofacial clefting: genetic brothers in arms?M Phan, F Conte, K D Khandelwal, et al.
Hormone Research in Paediatrics|April 3, 2015
Short Stature in KBG Syndrome: First Responses to Growth Hormone TreatmentNele Reynaert, C W Ockeloen, L Sävendahl, et al.
Clinical Genetics|April 6, 2013
Novel BCOR mutations in patients with oculofaciocardiodental (OFCD) syndromeH E Feberwee, I Feenstra, S Oberoi, et al.
Human Genetics|August 13, 2015
'Splitting versus lumping': Temple-Baraitser and Zimmermann-Laband SyndromesNuria C Bramswig, C W Ockeloen, J C Czeschik, et al.
Neuromuscular Disorders : NMD|May 8, 2012
Congenital myopathy caused by a novel missense mutation in the CFL2 geneC W Ockeloen, H J Gilhuis, R Pfundt, et al.
American Journal of Medical Genetics. Part A|June 24, 2025
An International ASXL3 Natural History Study: Deep Phenotypic Analyses Including Detailed Reports of a Milder Phenotype, Novel Associations, and Clinical RecommendationsE Woods, N Holmes, A S Denommé-Pichon, et al.
Molecular Syndromology|December 6, 2011
Sixteen New Cases Contributing to the Characterization of Patients with Distal 22q11.2 MicroduplicationsJ Wincent, D L Bruno, B W M van Bon, et al.
Pageof 1