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M Van Geel

Showing results (31-40 of 171) with videos related to

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Practical Radiation Oncology|July 17, 2021
Indeterminate Liver Lesions in Patients With Early Stage Rectal Cancer: Can They Be Ignored?Joris J van den Broek, Sabrine Q Kol, Jeroen Doodeman, et al.
The British Journal of Dermatology|July 12, 2008
Defects in DNA mismatch repair do not account for early-onset basal cell carcinomaK Mosterd, R G L Nellen, M van Engeland, et al.
Annals of the Rheumatic Diseases|August 5, 2008
Clinical subsequent fractures cluster in time after first fracturesT A C M van Geel, S van Helden, P P Geusens, et al.
Journal of Inherited Metabolic Disease|December 10, 2014
Hematopoietic cell transplantation does not prevent myelopathy in X-linked adrenoleukodystrophy: a retrospective studyBjörn M van Geel, Bwee Tien Poll-The, Aad Verrips, et al.
Experimental Dermatology|July 12, 2008
Granulomatous rosacea and Crohn's disease in a patient homozygous for the Crohn-associated NOD2/CARD15 polymorphism R702WM A M van Steensel, S Badeloe, V Winnepenninckx, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|July 27, 2001
Source and component genes of a 6-200 Mb gene cluster in the house mouseD Weichenhan, B Kunze, H Winking, et al.
Current Osteoporosis Reports|June 22, 2010
Assessment of individual fracture risk: FRAX and beyondJoop P W van den Bergh, Tineke A C M van Geel, Willem F Lems, et al.
Genomics|October 8, 1999
The FSHD region on human chromosome 4q35 contains potential coding regions among pseudogenes and a high density of repeat elementsM van Geel, L J Heather, R Lyle, et al.
American Journal of Medical Genetics. Part A|March 18, 2009
The missense mutation G12D in connexin30.3 can cause both erythrokeratodermia variabilis of Mendes da Costa and progressive symmetric erythrokeratodermia of GottronM A M van Steensel, A P Oranje, J G van der Schroeff, et al.
Maturitas|January 8, 2010
Individualizing fracture risk predictionTineke A C M van Geel, Joop P W van den Bergh, Geert-Jan Dinant, et al.
Pageof 18

Showing results (31-40 of 171) with videos related to

Sort By:
Pageof 18
Practical Radiation Oncology|July 17, 2021
Indeterminate Liver Lesions in Patients With Early Stage Rectal Cancer: Can They Be Ignored?Joris J van den Broek, Sabrine Q Kol, Jeroen Doodeman, et al.
The British Journal of Dermatology|July 12, 2008
Defects in DNA mismatch repair do not account for early-onset basal cell carcinomaK Mosterd, R G L Nellen, M van Engeland, et al.
Annals of the Rheumatic Diseases|August 5, 2008
Clinical subsequent fractures cluster in time after first fracturesT A C M van Geel, S van Helden, P P Geusens, et al.
Journal of Inherited Metabolic Disease|December 10, 2014
Hematopoietic cell transplantation does not prevent myelopathy in X-linked adrenoleukodystrophy: a retrospective studyBjörn M van Geel, Bwee Tien Poll-The, Aad Verrips, et al.
Experimental Dermatology|July 12, 2008
Granulomatous rosacea and Crohn's disease in a patient homozygous for the Crohn-associated NOD2/CARD15 polymorphism R702WM A M van Steensel, S Badeloe, V Winnepenninckx, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|July 27, 2001
Source and component genes of a 6-200 Mb gene cluster in the house mouseD Weichenhan, B Kunze, H Winking, et al.
Current Osteoporosis Reports|June 22, 2010
Assessment of individual fracture risk: FRAX and beyondJoop P W van den Bergh, Tineke A C M van Geel, Willem F Lems, et al.
Genomics|October 8, 1999
The FSHD region on human chromosome 4q35 contains potential coding regions among pseudogenes and a high density of repeat elementsM van Geel, L J Heather, R Lyle, et al.
American Journal of Medical Genetics. Part A|March 18, 2009
The missense mutation G12D in connexin30.3 can cause both erythrokeratodermia variabilis of Mendes da Costa and progressive symmetric erythrokeratodermia of GottronM A M van Steensel, A P Oranje, J G van der Schroeff, et al.
Maturitas|January 8, 2010
Individualizing fracture risk predictionTineke A C M van Geel, Joop P W van den Bergh, Geert-Jan Dinant, et al.
Pageof 18