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J Willems

Showing results (371-380 of 446) with videos related to

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Nature Genetics|January 1, 1993
A point mutation in the FMR-1 gene associated with fragile X mental retardationK De Boulle, A J Verkerk, E Reyniers, et al.
TAG. Theoretical and Applied Genetics. Theoretische Und Angewandte Genetik|February 22, 2023
Plasticity of maternal environment-dependent expression-QTLs of tomato seedsMark G Sterken, Harm Nijveen, Martijn van Zanten, et al.
Plant, Cell & Environment|March 19, 2016
Altitudinal and climatic associations of seed dormancy and flowering traits evidence adaptation of annual life cycle timing in Arabidopsis thalianaDeborah S Vidigal, Alexandre C S S Marques, Leo A J Willems, et al.
American Journal of Medical Genetics|August 9, 1996
Transgenic mouse model for the fragile X syndromeR F Kooy, R D'Hooge, E Reyniers, et al.
Genomics|April 1, 1991
Mapping of the gene for X-linked liver glycogenosis due to phosphorylase kinase deficiency to human chromosome region Xp22P J Willems, J Hendrickx, B J Van der Auwera, et al.
JAMA Network Open|February 23, 2023
Association of Proton Pump Inhibitor Use With Risk of Acquiring Drug-Resistant EnterobacteralesRoel P J Willems, Martijn C Schut, Anna M Kaiser, et al.
The Journal of Antimicrobial Chemotherapy|September 22, 2021
Gastric acid suppression, lifestyle factors and intestinal carriage of ESBL and carbapenemase-producing Enterobacterales: a nationwide population-based studyRoel P J Willems, Karin van Dijk, Cindy M Dierikx, et al.
Human Molecular Genetics|January 1, 1994
Assignment of a second locus for multiple exostoses to the pericentromeric region of chromosome 11Y Q Wu, P Heutink, B B de Vries, et al.
American Journal of Human Genetics|April 1, 1996
Delineation of a contiguous gene syndrome with multiple exostoses, enlarged parietal foramina, craniofacial dysostosis, and mental retardation, caused by deletions in the short arm of chromosome 11O Bartsch, W Wuyts, W Van Hul, et al.
Journal of Medical Genetics|May 11, 2010
Polyalanine expansion in the ZIC3 gene leading to X-linked heterotaxy with VACTERL association: a new polyalanine disorder?Marja W Wessels, Brian Kuchinka, Rogier Heydanus, et al.
Pageof 45

Showing results (371-380 of 446) with videos related to

Sort By:
Pageof 45
Nature Genetics|January 1, 1993
A point mutation in the FMR-1 gene associated with fragile X mental retardationK De Boulle, A J Verkerk, E Reyniers, et al.
TAG. Theoretical and Applied Genetics. Theoretische Und Angewandte Genetik|February 22, 2023
Plasticity of maternal environment-dependent expression-QTLs of tomato seedsMark G Sterken, Harm Nijveen, Martijn van Zanten, et al.
Plant, Cell & Environment|March 19, 2016
Altitudinal and climatic associations of seed dormancy and flowering traits evidence adaptation of annual life cycle timing in Arabidopsis thalianaDeborah S Vidigal, Alexandre C S S Marques, Leo A J Willems, et al.
American Journal of Medical Genetics|August 9, 1996
Transgenic mouse model for the fragile X syndromeR F Kooy, R D'Hooge, E Reyniers, et al.
Genomics|April 1, 1991
Mapping of the gene for X-linked liver glycogenosis due to phosphorylase kinase deficiency to human chromosome region Xp22P J Willems, J Hendrickx, B J Van der Auwera, et al.
JAMA Network Open|February 23, 2023
Association of Proton Pump Inhibitor Use With Risk of Acquiring Drug-Resistant EnterobacteralesRoel P J Willems, Martijn C Schut, Anna M Kaiser, et al.
The Journal of Antimicrobial Chemotherapy|September 22, 2021
Gastric acid suppression, lifestyle factors and intestinal carriage of ESBL and carbapenemase-producing Enterobacterales: a nationwide population-based studyRoel P J Willems, Karin van Dijk, Cindy M Dierikx, et al.
Human Molecular Genetics|January 1, 1994
Assignment of a second locus for multiple exostoses to the pericentromeric region of chromosome 11Y Q Wu, P Heutink, B B de Vries, et al.
American Journal of Human Genetics|April 1, 1996
Delineation of a contiguous gene syndrome with multiple exostoses, enlarged parietal foramina, craniofacial dysostosis, and mental retardation, caused by deletions in the short arm of chromosome 11O Bartsch, W Wuyts, W Van Hul, et al.
Journal of Medical Genetics|May 11, 2010
Polyalanine expansion in the ZIC3 gene leading to X-linked heterotaxy with VACTERL association: a new polyalanine disorder?Marja W Wessels, Brian Kuchinka, Rogier Heydanus, et al.
Pageof 45