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

G Matthijs

Showing results (31-40 of 157) with videos related to

Pageof 16
Sort By:
Clinical Genetics|October 12, 1999
Association between CAG repeat number in the androgen receptor and male infertility in a Belgian studyE Legius, D Vanderschueren, C Spiessens, et al.
FEBS Letters|July 14, 1997
Comparison of PMM1 with the phosphomannomutases expressed in rat liver and in human cellsM Pirard, J F Collet, G Matthijs, et al.
European Journal of Pediatrics|December 29, 2000
Preaxial polydactyly type 1 and severe language deficit in maternal uniparental disomy of chromosome 7S Potgieter, G Matthijs, P De Cock, et al.
Biochemical and Biophysical Research Communications|June 6, 1995
A regulatory element in the 5'UTR directs cell-specific expression of the mouse alpha 4 geneE Schollen, C De Meirsman, G Matthijs, et al.
European Journal of Human Genetics : EJHG|January 1, 1996
Non-syndromic deafness associated with a mutation and a polymorphism in the mitochondrial 12S ribosomal RNA gene in a large Zairean pedigreeG Matthijs, S Claes, B Longo-Mbenza, et al.
Journal of Medical Genetics|January 15, 2003
Chromosome 15 maternal uniparental disomy and psychosis in Prader-Willi syndromeA Vogels, G Matthijs, E Legius, et al.
American Journal of Human Genetics|January 13, 2001
High residual activity of PMM2 in patients' fibroblasts: possible pitfall in the diagnosis of CDG-Ia (phosphomannomutase deficiency)S Grünewald, E Schollen, E Van Schaftingen, et al.
European Journal of Human Genetics : EJHG|August 10, 1999
Mutational analysis of the Cu/Zn superoxide dismutase gene in 23 familial and 69 sporadic cases of amyotrophic lateral sclerosis in BelgiumT Aguirre, G Matthijs, W Robberecht, et al.
Human Mutation|July 23, 2003
Gross rearrangements in the MECP2 gene in three patients with Rett syndrome: implications for routine diagnosis of Rett syndromeE Schollen, E Smeets, E Deflem, et al.
Biochemical and Biophysical Research Communications|July 15, 1994
Characterization of the human alpha 2-macroglobulin gene promoter: identification of a novel, triple TRE/RARE/ERE response elementG Matthijs, J J Cassiman, H Van den Berghe, et al.
Pageof 16

Showing results (31-40 of 157) with videos related to

Sort By:
Pageof 16
Clinical Genetics|October 12, 1999
Association between CAG repeat number in the androgen receptor and male infertility in a Belgian studyE Legius, D Vanderschueren, C Spiessens, et al.
FEBS Letters|July 14, 1997
Comparison of PMM1 with the phosphomannomutases expressed in rat liver and in human cellsM Pirard, J F Collet, G Matthijs, et al.
European Journal of Pediatrics|December 29, 2000
Preaxial polydactyly type 1 and severe language deficit in maternal uniparental disomy of chromosome 7S Potgieter, G Matthijs, P De Cock, et al.
Biochemical and Biophysical Research Communications|June 6, 1995
A regulatory element in the 5'UTR directs cell-specific expression of the mouse alpha 4 geneE Schollen, C De Meirsman, G Matthijs, et al.
European Journal of Human Genetics : EJHG|January 1, 1996
Non-syndromic deafness associated with a mutation and a polymorphism in the mitochondrial 12S ribosomal RNA gene in a large Zairean pedigreeG Matthijs, S Claes, B Longo-Mbenza, et al.
Journal of Medical Genetics|January 15, 2003
Chromosome 15 maternal uniparental disomy and psychosis in Prader-Willi syndromeA Vogels, G Matthijs, E Legius, et al.
American Journal of Human Genetics|January 13, 2001
High residual activity of PMM2 in patients' fibroblasts: possible pitfall in the diagnosis of CDG-Ia (phosphomannomutase deficiency)S Grünewald, E Schollen, E Van Schaftingen, et al.
European Journal of Human Genetics : EJHG|August 10, 1999
Mutational analysis of the Cu/Zn superoxide dismutase gene in 23 familial and 69 sporadic cases of amyotrophic lateral sclerosis in BelgiumT Aguirre, G Matthijs, W Robberecht, et al.
Human Mutation|July 23, 2003
Gross rearrangements in the MECP2 gene in three patients with Rett syndrome: implications for routine diagnosis of Rett syndromeE Schollen, E Smeets, E Deflem, et al.
Biochemical and Biophysical Research Communications|July 15, 1994
Characterization of the human alpha 2-macroglobulin gene promoter: identification of a novel, triple TRE/RARE/ERE response elementG Matthijs, J J Cassiman, H Van den Berghe, et al.
Pageof 16