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M Goossens

Showing results (281-290 of 364) with videos related to

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International Journal for Equity in Health|November 28, 2020
Coverage determinants of breast cancer screening in Flanders: an evaluation of the past decadeL Ding, S Jidkova, M J W Greuter, et al.
Annals of Human Genetics|January 11, 2005
Comprehensive cystic fibrosis mutation epidemiology and haplotype characterization in a southern Italian populationG Castaldo, A Polizzi, R Tomaiuolo, et al.
Leukemia|February 1, 1990
Frequent detection of minimal residual disease by use of the polymerase chain reaction in long-term survivors after bone marrow transplantation for chronic myeloid leukemiaJ M Pignon, T Henni, S Amselem, et al.
Annals of the Rheumatic Diseases|July 24, 2004
Large differences in cost of illness and wellbeing between patients with fibromyalgia, chronic low back pain, or ankylosing spondylitisA Boonen, R van den Heuvel, A van Tubergen, et al.
Nature Genetics|November 1, 1993
A homozygous insertion-deletion in the type VII collagen gene (COL7A1) in Hallopeau-Siemens dystrophic epidermolysis bullosaL Hilal, A Rochat, P Duquesnoy, et al.
Genomics|February 1, 1992
A nonsense mutation (R1158X) and a splicing mutation (3849 + 4A----G) in exon 19 of the cystic fibrosis transmembrane conductance regulator geneP Ronchetto, J J Telleria Orriols, P Fanen, et al.
Blood|June 1, 1980
The detection and use of hemoglobin mutants in the direct analysis of human globin genesP F Little, E Whitelaw, G Annison, et al.
FEBS Letters|August 28, 1998
Expression of the SOX10 gene during human developmentN Bondurand, A Kobetz, V Pingault, et al.
The EMBO Journal|September 1, 1986
Molecular cloning and sequencing of the human erythrocyte 2,3-bisphosphoglycerate mutase cDNA: revised amino acid sequenceV Joulin, J Peduzzi, P H Roméo, et al.
Oncogene|December 1, 1991
Mutations in the p53 gene in myelodysplastic syndromesP Jonveaux, P Fenaux, I Quiquandon, et al.
Pageof 37

Showing results (281-290 of 364) with videos related to

Sort By:
Pageof 37
International Journal for Equity in Health|November 28, 2020
Coverage determinants of breast cancer screening in Flanders: an evaluation of the past decadeL Ding, S Jidkova, M J W Greuter, et al.
Annals of Human Genetics|January 11, 2005
Comprehensive cystic fibrosis mutation epidemiology and haplotype characterization in a southern Italian populationG Castaldo, A Polizzi, R Tomaiuolo, et al.
Leukemia|February 1, 1990
Frequent detection of minimal residual disease by use of the polymerase chain reaction in long-term survivors after bone marrow transplantation for chronic myeloid leukemiaJ M Pignon, T Henni, S Amselem, et al.
Annals of the Rheumatic Diseases|July 24, 2004
Large differences in cost of illness and wellbeing between patients with fibromyalgia, chronic low back pain, or ankylosing spondylitisA Boonen, R van den Heuvel, A van Tubergen, et al.
Nature Genetics|November 1, 1993
A homozygous insertion-deletion in the type VII collagen gene (COL7A1) in Hallopeau-Siemens dystrophic epidermolysis bullosaL Hilal, A Rochat, P Duquesnoy, et al.
Genomics|February 1, 1992
A nonsense mutation (R1158X) and a splicing mutation (3849 + 4A----G) in exon 19 of the cystic fibrosis transmembrane conductance regulator geneP Ronchetto, J J Telleria Orriols, P Fanen, et al.
Blood|June 1, 1980
The detection and use of hemoglobin mutants in the direct analysis of human globin genesP F Little, E Whitelaw, G Annison, et al.
FEBS Letters|August 28, 1998
Expression of the SOX10 gene during human developmentN Bondurand, A Kobetz, V Pingault, et al.
The EMBO Journal|September 1, 1986
Molecular cloning and sequencing of the human erythrocyte 2,3-bisphosphoglycerate mutase cDNA: revised amino acid sequenceV Joulin, J Peduzzi, P H Roméo, et al.
Oncogene|December 1, 1991
Mutations in the p53 gene in myelodysplastic syndromesP Jonveaux, P Fenaux, I Quiquandon, et al.
Pageof 37