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

Miikka Vikkula

Showing results (71-80 of 199) with videos related to

Pageof 20
Sort By:
Genes|October 27, 2019
Likely Pathogenic Variants in One Third of Non-Syndromic Discontinuous Cleft Lip and Palate PatientsBénédicte Demeer, Nicole Revencu, Raphael Helaers, et al.
American Journal of Medical Genetics. Part A|June 1, 2011
5q14.3 neurocutaneous syndrome: a novel continguous gene syndrome caused by simultaneous deletion of RASA1 and MEF2CChristopher W Carr, Holly H Zimmerman, Christa Lese Martin, et al.
American Journal of Human Genetics|November 26, 2003
Capillary malformation-arteriovenous malformation, a new clinical and genetic disorder caused by RASA1 mutationsIiro Eerola, Laurence M Boon, John B Mulliken, et al.
Human Molecular Genetics|June 19, 2008
PTHR1 mutations associated with Ollier disease result in receptor loss of functionAlain Couvineau, Vinciane Wouters, Guylène Bertrand, et al.
Dermatology (Basel, Switzerland)|February 3, 2009
Cutaneous venous malformations in familial cerebral cavernomatosis caused by KRIT1 gene mutationsAgustí Toll, Elisabet Parera, Ana M Giménez-Arnau, et al.
Diagnostic and Interventional Imaging|August 2, 2024
Injectable chitosan hydrogel effectively controls lesion growth in a venous malformation murine modelHa-Long Nguyen, Ricardo Holderbaum Do Amaral, Sophie Lerouge, et al.
European Journal of Human Genetics : EJHG|November 6, 2024
Four putative pathogenic ARHGAP29 variants in patients with non-syndromic orofacial clefts (NsOFC)Peyman Ranji, Eleonore Pairet, Raphael Helaers, et al.
American Journal of Human Genetics|December 7, 2015
Somatic Activating PIK3CA Mutations Cause Venous MalformationNisha Limaye, Jaakko Kangas, Antonella Mendola, et al.
Cancer Medicine|April 27, 2019
DNA alteration-based classification of uveal melanoma gives better prognostic stratification than immune infiltration, which has a neutral effect in high-risk groupDeepti Narasimhaiah, Catherine Legrand, Diane Damotte, et al.
Cancer Genetics|January 19, 2016
The peculiar 11q-gain/loss aberration reported in a subset of MYC-negative high-grade B-cell lymphomas can also occur in a MYC-rearranged lymphomaViolaine Havelange, Geneviève Ameye, Ivan Théate, et al.
Pageof 20

Showing results (71-80 of 199) with videos related to

Sort By:
Pageof 20
Genes|October 27, 2019
Likely Pathogenic Variants in One Third of Non-Syndromic Discontinuous Cleft Lip and Palate PatientsBénédicte Demeer, Nicole Revencu, Raphael Helaers, et al.
American Journal of Medical Genetics. Part A|June 1, 2011
5q14.3 neurocutaneous syndrome: a novel continguous gene syndrome caused by simultaneous deletion of RASA1 and MEF2CChristopher W Carr, Holly H Zimmerman, Christa Lese Martin, et al.
American Journal of Human Genetics|November 26, 2003
Capillary malformation-arteriovenous malformation, a new clinical and genetic disorder caused by RASA1 mutationsIiro Eerola, Laurence M Boon, John B Mulliken, et al.
Human Molecular Genetics|June 19, 2008
PTHR1 mutations associated with Ollier disease result in receptor loss of functionAlain Couvineau, Vinciane Wouters, Guylène Bertrand, et al.
Dermatology (Basel, Switzerland)|February 3, 2009
Cutaneous venous malformations in familial cerebral cavernomatosis caused by KRIT1 gene mutationsAgustí Toll, Elisabet Parera, Ana M Giménez-Arnau, et al.
Diagnostic and Interventional Imaging|August 2, 2024
Injectable chitosan hydrogel effectively controls lesion growth in a venous malformation murine modelHa-Long Nguyen, Ricardo Holderbaum Do Amaral, Sophie Lerouge, et al.
European Journal of Human Genetics : EJHG|November 6, 2024
Four putative pathogenic ARHGAP29 variants in patients with non-syndromic orofacial clefts (NsOFC)Peyman Ranji, Eleonore Pairet, Raphael Helaers, et al.
American Journal of Human Genetics|December 7, 2015
Somatic Activating PIK3CA Mutations Cause Venous MalformationNisha Limaye, Jaakko Kangas, Antonella Mendola, et al.
Cancer Medicine|April 27, 2019
DNA alteration-based classification of uveal melanoma gives better prognostic stratification than immune infiltration, which has a neutral effect in high-risk groupDeepti Narasimhaiah, Catherine Legrand, Diane Damotte, et al.
Cancer Genetics|January 19, 2016
The peculiar 11q-gain/loss aberration reported in a subset of MYC-negative high-grade B-cell lymphomas can also occur in a MYC-rearranged lymphomaViolaine Havelange, Geneviève Ameye, Ivan Théate, et al.
Pageof 20