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M Vikkula

Showing results (21-30 of 57) with videos related to

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Lymphology|April 17, 2025
Updated Human Chromosome Map of Lymphedema-lymphangiogenesis Genes: Template for Current and Future DiscoveryP Brouillard, M H Witte, R P Erickson, et al.
Lymphology|January 24, 2022
Human chromosome map of lymphedema-lymphangiogenesis genes: Template for current and future discoveryM H Witte, R P Erickson, L Luy, et al.
Genomics|April 1, 1993
A mutation in the amino-terminal end of the triple helix of type II collagen causing severe osteochondrodysplasiaM Vikkula, P Ritvaniemi, A F Vuorio, et al.
The Biochemical Journal|July 1, 1992
Structural analysis of the regulatory elements of the type-II procollagen gene. Conservation of promoter and first intron sequences between human and mouseM Vikkula, M Metsäranta, A C Syvänen, et al.
Annals of the Rheumatic Diseases|October 1, 1993
Multiallelic polymorphism of the cartilage collagen gene: no association with osteoarthrosisM Vikkula, M Nissilä, E Hirvensalo, et al.
Human Molecular Genetics|May 18, 2000
KRIT1 is mutated in hyperkeratotic cutaneous capillary-venous malformation associated with cerebral capillary malformationI Eerola, K H Plate, R Spiegel, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|May 13, 2015
Tandem inversion duplication within F8 Intron 1 associated with mild haemophilia AN Lannoy, C Bandelier, B Grisart, et al.
Journal of Medical Genetics|March 18, 2009
Recessive primary congenital lymphoedema caused by a VEGFR3 mutationA Ghalamkarpour, W Holnthoner, P Saharinen, et al.
Clinical Genetics|September 13, 2006
Hereditary lymphedema type I associated with VEGFR3 mutation: the first de novo case and atypical presentationsA Ghalamkarpour, S Morlot, A Raas-Rothschild, et al.
Arthritis and Rheumatism|March 1, 1993
Early-onset osteoarthritis linked to the type II procollagen gene. Detailed clinical phenotype and further analyses of the geneM Vikkula, A Palotie, P Ritvaniemi, et al.
Pageof 6

Showing results (21-30 of 57) with videos related to

Sort By:
Pageof 6
Lymphology|April 17, 2025
Updated Human Chromosome Map of Lymphedema-lymphangiogenesis Genes: Template for Current and Future DiscoveryP Brouillard, M H Witte, R P Erickson, et al.
Lymphology|January 24, 2022
Human chromosome map of lymphedema-lymphangiogenesis genes: Template for current and future discoveryM H Witte, R P Erickson, L Luy, et al.
Genomics|April 1, 1993
A mutation in the amino-terminal end of the triple helix of type II collagen causing severe osteochondrodysplasiaM Vikkula, P Ritvaniemi, A F Vuorio, et al.
The Biochemical Journal|July 1, 1992
Structural analysis of the regulatory elements of the type-II procollagen gene. Conservation of promoter and first intron sequences between human and mouseM Vikkula, M Metsäranta, A C Syvänen, et al.
Annals of the Rheumatic Diseases|October 1, 1993
Multiallelic polymorphism of the cartilage collagen gene: no association with osteoarthrosisM Vikkula, M Nissilä, E Hirvensalo, et al.
Human Molecular Genetics|May 18, 2000
KRIT1 is mutated in hyperkeratotic cutaneous capillary-venous malformation associated with cerebral capillary malformationI Eerola, K H Plate, R Spiegel, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|May 13, 2015
Tandem inversion duplication within F8 Intron 1 associated with mild haemophilia AN Lannoy, C Bandelier, B Grisart, et al.
Journal of Medical Genetics|March 18, 2009
Recessive primary congenital lymphoedema caused by a VEGFR3 mutationA Ghalamkarpour, W Holnthoner, P Saharinen, et al.
Clinical Genetics|September 13, 2006
Hereditary lymphedema type I associated with VEGFR3 mutation: the first de novo case and atypical presentationsA Ghalamkarpour, S Morlot, A Raas-Rothschild, et al.
Arthritis and Rheumatism|March 1, 1993
Early-onset osteoarthritis linked to the type II procollagen gene. Detailed clinical phenotype and further analyses of the geneM Vikkula, A Palotie, P Ritvaniemi, et al.
Pageof 6