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

M Vikkula

Showing results (31-40 of 57) with videos related to

Pageof 6
Sort By:
Clinical Genetics|April 5, 2014
Hypotrichosis-lymphedema-telangiectasia-renal defect associated with a truncating mutation in the SOX18 geneS Moalem, P Brouillard, D Kuypers, et al.
Neuropathology and Applied Neurobiology|November 26, 2003
CDKN2A, CDKN2B and p14ARF are frequently and differentially methylated in ependymal tumoursE Rousseau, M-M Ruchoux, F Scaravilli, et al.
Human Molecular Genetics|September 1, 1994
Assignment of a locus for dominantly inherited venous malformations to chromosome 9pL M Boon, J B Mulliken, M Vikkula, et al.
Lancet (London, England)|April 29, 1989
Predisposition to familial osteoarthrosis linked to type II collagen geneA Palotie, P Väisänen, J Ott, et al.
Journal of Immunology (Baltimore, Md. : 1950)|May 23, 2000
High frequency of autologous anti-melanoma CTL directed against an antigen generated by a point mutation in a new helicase geneJ F Baurain, D Colau, N van Baren, et al.
B-ENT|March 21, 2007
Orofacial clefting: update on the role of geneticsM Ghassibe, B Bayet, N Revencu, et al.
European Journal of Medical Genetics|April 22, 2015
Antenatal presentation of hereditary lymphedema type IE Boudon, Y Levy, T Abossolo, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|May 9, 2012
Prevalence and spectrum of SDHx mutations in pheochromocytoma and paraganglioma in patients from Belgium: an updateA Persu, N Lannoy, D Maiter, et al.
Arthritis and Rheumatism|July 1, 1995
Identification of COL2A1 gene mutations in patients with chondrodysplasias and familial osteoarthritisP Ritvaniemi, J Körkkö, J Bonaventure, et al.
American Journal of Human Genetics|June 12, 1999
A gene for inherited cutaneous venous anomalies ("glomangiomas") localizes to chromosome 1p21-22L M Boon, P Brouillard, A Irrthum, et al.
Pageof 6

Showing results (31-40 of 57) with videos related to

Sort By:
Pageof 6
Clinical Genetics|April 5, 2014
Hypotrichosis-lymphedema-telangiectasia-renal defect associated with a truncating mutation in the SOX18 geneS Moalem, P Brouillard, D Kuypers, et al.
Neuropathology and Applied Neurobiology|November 26, 2003
CDKN2A, CDKN2B and p14ARF are frequently and differentially methylated in ependymal tumoursE Rousseau, M-M Ruchoux, F Scaravilli, et al.
Human Molecular Genetics|September 1, 1994
Assignment of a locus for dominantly inherited venous malformations to chromosome 9pL M Boon, J B Mulliken, M Vikkula, et al.
Lancet (London, England)|April 29, 1989
Predisposition to familial osteoarthrosis linked to type II collagen geneA Palotie, P Väisänen, J Ott, et al.
Journal of Immunology (Baltimore, Md. : 1950)|May 23, 2000
High frequency of autologous anti-melanoma CTL directed against an antigen generated by a point mutation in a new helicase geneJ F Baurain, D Colau, N van Baren, et al.
B-ENT|March 21, 2007
Orofacial clefting: update on the role of geneticsM Ghassibe, B Bayet, N Revencu, et al.
European Journal of Medical Genetics|April 22, 2015
Antenatal presentation of hereditary lymphedema type IE Boudon, Y Levy, T Abossolo, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|May 9, 2012
Prevalence and spectrum of SDHx mutations in pheochromocytoma and paraganglioma in patients from Belgium: an updateA Persu, N Lannoy, D Maiter, et al.
Arthritis and Rheumatism|July 1, 1995
Identification of COL2A1 gene mutations in patients with chondrodysplasias and familial osteoarthritisP Ritvaniemi, J Körkkö, J Bonaventure, et al.
American Journal of Human Genetics|June 12, 1999
A gene for inherited cutaneous venous anomalies ("glomangiomas") localizes to chromosome 1p21-22L M Boon, P Brouillard, A Irrthum, et al.
Pageof 6