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M Goossens

Showing results (271-280 of 364) with videos related to

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Surgical Technology International|May 14, 2016
Comparative Study of Performance in Ultrasonic Tissue Dissection for Sleeve Gastrectomy: Wired versus CordlessPim W J van Rutte, Sandra L Lup, Misha D Luyer, et al.
Journal of Neurology|August 14, 2001
The SOX10 transcription factor: evaluation as a candidate gene for central and peripheral hereditary myelin disordersV Pingault, N Bondurand, C Le Caignec, et al.
Progress in Clinical and Biological Research|January 1, 1981
New techniques for the prenatal diagnosis of hemoglobinopathiesA Dubart, Y Blouquit, M Goossens, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|May 1, 1994
Hb Taybe (alpha 38 or 39 THR deleted): an alpha-globin defect, silent in the heterozygous state and producing severe hemolytic anemia in the homozygousF Galacteros, E Girodon, A M'Rad, et al.
Journal of the American Veterinary Medical Association|August 14, 1998
Cobalt 60 irradiation of pituitary gland tumors in three cats with acromegalyM M Goossens, E C Feldman, R W Nelson, et al.
European Journal of Human Genetics : EJHG|January 1, 1993
Haemophilia B due to a de novo insertion of a human-specific Alu subfamily member within the coding region of the factor IX geneD Vidaud, M Vidaud, B R Bahnak, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 1, 1989
Tissue-specific splicing mutation in acute intermittent porphyriaB Grandchamp, C Picat, V Mignotte, et al.
American Journal of Human Genetics|December 1, 1999
Loss-of-function mutations in a human gene related to Chlamydomonas reinhardtii dynein IC78 result in primary ciliary dyskinesiaG Pennarun, E Escudier, C Chapelin, et al.
Preventive Medicine|December 3, 2014
Quantifying independent risk factors for failing to rescreen in a breast cancer screening program in Flanders, BelgiumM Goossens, G Van Hal, M Van der Burg, et al.
British Journal of Haematology|December 1, 1988
Identification of a CpG mutation in the coagulation factor-IX gene by analysis of amplified DNA sequencesV Siguret, S Amselem, M Vidaud, et al.
Pageof 37

Showing results (271-280 of 364) with videos related to

Sort By:
Pageof 37
Surgical Technology International|May 14, 2016
Comparative Study of Performance in Ultrasonic Tissue Dissection for Sleeve Gastrectomy: Wired versus CordlessPim W J van Rutte, Sandra L Lup, Misha D Luyer, et al.
Journal of Neurology|August 14, 2001
The SOX10 transcription factor: evaluation as a candidate gene for central and peripheral hereditary myelin disordersV Pingault, N Bondurand, C Le Caignec, et al.
Progress in Clinical and Biological Research|January 1, 1981
New techniques for the prenatal diagnosis of hemoglobinopathiesA Dubart, Y Blouquit, M Goossens, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|May 1, 1994
Hb Taybe (alpha 38 or 39 THR deleted): an alpha-globin defect, silent in the heterozygous state and producing severe hemolytic anemia in the homozygousF Galacteros, E Girodon, A M'Rad, et al.
Journal of the American Veterinary Medical Association|August 14, 1998
Cobalt 60 irradiation of pituitary gland tumors in three cats with acromegalyM M Goossens, E C Feldman, R W Nelson, et al.
European Journal of Human Genetics : EJHG|January 1, 1993
Haemophilia B due to a de novo insertion of a human-specific Alu subfamily member within the coding region of the factor IX geneD Vidaud, M Vidaud, B R Bahnak, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 1, 1989
Tissue-specific splicing mutation in acute intermittent porphyriaB Grandchamp, C Picat, V Mignotte, et al.
American Journal of Human Genetics|December 1, 1999
Loss-of-function mutations in a human gene related to Chlamydomonas reinhardtii dynein IC78 result in primary ciliary dyskinesiaG Pennarun, E Escudier, C Chapelin, et al.
Preventive Medicine|December 3, 2014
Quantifying independent risk factors for failing to rescreen in a breast cancer screening program in Flanders, BelgiumM Goossens, G Van Hal, M Van der Burg, et al.
British Journal of Haematology|December 1, 1988
Identification of a CpG mutation in the coagulation factor-IX gene by analysis of amplified DNA sequencesV Siguret, S Amselem, M Vidaud, et al.
Pageof 37