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L Nuytinck

Showing results (21-30 of 33) with videos related to

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American Journal of Human Genetics|March 7, 1998
Analysis of the COL1A1 and COL1A2 genes by PCR amplification and scanning by conformation-sensitive gel electrophoresis identifies only COL1A1 mutations in 15 patients with osteogenesis imperfecta type I: identification of common sequences of null-allele mutationsJ Körkkö, L Ala-Kokko, A De Paepe, et al.
Clinical and Experimental Dermatology|November 28, 2001
Characterization of mutations leading to recessive dystrophic epidermolysis bullosa and Marfan syndrome in a single patientR Gardella, L Nuytinck, S Barlati, et al.
Human Mutation|July 9, 2004
Comprehensive molecular screening of the FBN1 gene favors locus homogeneity of classical Marfan syndromeB Loeys, J De Backer, P Van Acker, et al.
Nature Genetics|June 1, 1992
Evidence for a relationship between Ehlers-Danlos type VII C in humans and bovine dermatosparaxisB V Nusgens, C Verellen-Dumoulin, T Hermanns-Lê, et al.
Pediatric Radiology|November 3, 1998
Bruck syndrome: neonatal presentation and natural course in three patientsJ G Leroy, L Nuytinck, A De Paepe, et al.
Prenatal Diagnosis|January 26, 2002
Strategies for prenatal and preimplantation genetic diagnosis in Marfan syndrome (MFS)B Loeys, L Nuytinck, P Van Acker, et al.
Clinical and Experimental Immunology|August 8, 2007
Extremes of L-ficolin concentration in children with recurrent infections are associated with single nucleotide polymorphisms in the FCN2 geneM Cedzynski, L Nuytinck, A P M Atkinson, et al.
Rheumatology (Oxford, England)|November 23, 2007
Polymorphisms in the ficolin 1 gene (FCN1) are associated with susceptibility to the development of rheumatoid arthritisB Vander Cruyssen, L Nuytinck, L Boullart, et al.
Acta Clinica Belgica|December 6, 2023
The development of the Belgian paediatric clinical trial networkE Degraeuwe, L Persijn, L Nuytinck, et al.
Human Immunology|September 3, 2013
Genetic variations in toll-like receptor pathway and lung function decline in Cystic fibrosis patientsF Haerynck, J M Mahachie John, K Van Steen, et al.
Pageof 4

Showing results (21-30 of 33) with videos related to

Sort By:
Pageof 4
American Journal of Human Genetics|March 7, 1998
Analysis of the COL1A1 and COL1A2 genes by PCR amplification and scanning by conformation-sensitive gel electrophoresis identifies only COL1A1 mutations in 15 patients with osteogenesis imperfecta type I: identification of common sequences of null-allele mutationsJ Körkkö, L Ala-Kokko, A De Paepe, et al.
Clinical and Experimental Dermatology|November 28, 2001
Characterization of mutations leading to recessive dystrophic epidermolysis bullosa and Marfan syndrome in a single patientR Gardella, L Nuytinck, S Barlati, et al.
Human Mutation|July 9, 2004
Comprehensive molecular screening of the FBN1 gene favors locus homogeneity of classical Marfan syndromeB Loeys, J De Backer, P Van Acker, et al.
Nature Genetics|June 1, 1992
Evidence for a relationship between Ehlers-Danlos type VII C in humans and bovine dermatosparaxisB V Nusgens, C Verellen-Dumoulin, T Hermanns-Lê, et al.
Pediatric Radiology|November 3, 1998
Bruck syndrome: neonatal presentation and natural course in three patientsJ G Leroy, L Nuytinck, A De Paepe, et al.
Prenatal Diagnosis|January 26, 2002
Strategies for prenatal and preimplantation genetic diagnosis in Marfan syndrome (MFS)B Loeys, L Nuytinck, P Van Acker, et al.
Clinical and Experimental Immunology|August 8, 2007
Extremes of L-ficolin concentration in children with recurrent infections are associated with single nucleotide polymorphisms in the FCN2 geneM Cedzynski, L Nuytinck, A P M Atkinson, et al.
Rheumatology (Oxford, England)|November 23, 2007
Polymorphisms in the ficolin 1 gene (FCN1) are associated with susceptibility to the development of rheumatoid arthritisB Vander Cruyssen, L Nuytinck, L Boullart, et al.
Acta Clinica Belgica|December 6, 2023
The development of the Belgian paediatric clinical trial networkE Degraeuwe, L Persijn, L Nuytinck, et al.
Human Immunology|September 3, 2013
Genetic variations in toll-like receptor pathway and lung function decline in Cystic fibrosis patientsF Haerynck, J M Mahachie John, K Van Steen, et al.
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