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Nature Genetics
|
January 1, 1993
A point mutation in the FMR-1 gene associated with fragile X mental retardation
K 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 seeds
Mark 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 thaliana
Deborah 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 syndrome
R 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 Xp22
P 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 Enterobacterales
Roel 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 study
Roel 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 11
Y 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 11
O 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.
Page
of 45
Search research articles
Search
Showing results (371-380 of 446) with videos related to
Sort By:
Page
of 45
Nature Genetics
|
January 1, 1993
A point mutation in the FMR-1 gene associated with fragile X mental retardation
K 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 seeds
Mark 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 thaliana
Deborah 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 syndrome
R 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 Xp22
P 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 Enterobacterales
Roel 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 study
Roel 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 11
Y 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 11
O 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.
Page
of 45