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International Journal of Psychophysiology : Official Journal of the International Organization of Psychophysiology
|
June 12, 2010
The P300 event-related potential and smoking--a population-based case-control study
A Mobascher, J Brinkmeyer, T Warbrick, et al.
Genome Medicine
|
February 7, 2013
De novo truncating mutations in ASXL3 are associated with a novel clinical phenotype with similarities to Bohring-Opitz syndrome
Matthew N Bainbridge, Hao Hu, Donna M Muzny, et al.
European Radiology Experimental
|
December 5, 2024
Fully automatic quantification of pulmonary fat attenuation volume by CT: an exploratory pilot study
Luca Salhöfer, Mathias Holtkamp, Francesco Bonella, et al.
Plos One
|
April 8, 2016
Association of Common Polymorphisms in the Nicotinic Acetylcholine Receptor Alpha4 Subunit Gene with an Electrophysiological Endophenotype in a Large Population-Based Sample
A Mobascher, A Diaz-Lacava, M Wagner, et al.
Addiction Biology
|
August 24, 2012
Impaired sleep quality and sleep duration in smokers-results from the German Multicenter Study on Nicotine Dependence
Stefan Cohrs, Andrea Rodenbeck, Dieter Riemann, et al.
American Journal of Human Genetics
|
February 11, 1999
Limb mammary syndrome: a new genetic disorder with mammary hypoplasia, ectrodactyly, and other Hand/Foot anomalies maps to human chromosome 3q27
H van Bokhoven, M Jung, A P Smits, et al.
American Journal of Medical Genetics. Part A
|
August 16, 2014
NDST1 missense mutations in autosomal recessive intellectual disability
Miriam S Reuter, Luciana Musante, Hao Hu, et al.
Biological Psychiatry
|
July 1, 2008
The opioid peptides enkephalin and beta-endorphin in alcohol dependence
Ildiko Racz, Britta Schürmann, Anna Karpushova, et al.
The European Respiratory Journal
|
February 6, 2025
First assessment of photon-counting CT for virtual bronchoscopic navigation
Marcel Opitz, Faustina Funke, Kaid Darwiche, et al.
American Journal of Human Genetics
|
May 4, 2000
A gene for hypotrichosis simplex of the scalp maps to chromosome 6p21.3
R C Betz, Y A Lee, A Bygum, et al.
Page
of 29
Search research articles
Search
Showing results (211-220 of 282) with videos related to
Sort By:
Page
of 29
International Journal of Psychophysiology : Official Journal of the International Organization of Psychophysiology
|
June 12, 2010
The P300 event-related potential and smoking--a population-based case-control study
A Mobascher, J Brinkmeyer, T Warbrick, et al.
Genome Medicine
|
February 7, 2013
De novo truncating mutations in ASXL3 are associated with a novel clinical phenotype with similarities to Bohring-Opitz syndrome
Matthew N Bainbridge, Hao Hu, Donna M Muzny, et al.
European Radiology Experimental
|
December 5, 2024
Fully automatic quantification of pulmonary fat attenuation volume by CT: an exploratory pilot study
Luca Salhöfer, Mathias Holtkamp, Francesco Bonella, et al.
Plos One
|
April 8, 2016
Association of Common Polymorphisms in the Nicotinic Acetylcholine Receptor Alpha4 Subunit Gene with an Electrophysiological Endophenotype in a Large Population-Based Sample
A Mobascher, A Diaz-Lacava, M Wagner, et al.
Addiction Biology
|
August 24, 2012
Impaired sleep quality and sleep duration in smokers-results from the German Multicenter Study on Nicotine Dependence
Stefan Cohrs, Andrea Rodenbeck, Dieter Riemann, et al.
American Journal of Human Genetics
|
February 11, 1999
Limb mammary syndrome: a new genetic disorder with mammary hypoplasia, ectrodactyly, and other Hand/Foot anomalies maps to human chromosome 3q27
H van Bokhoven, M Jung, A P Smits, et al.
American Journal of Medical Genetics. Part A
|
August 16, 2014
NDST1 missense mutations in autosomal recessive intellectual disability
Miriam S Reuter, Luciana Musante, Hao Hu, et al.
Biological Psychiatry
|
July 1, 2008
The opioid peptides enkephalin and beta-endorphin in alcohol dependence
Ildiko Racz, Britta Schürmann, Anna Karpushova, et al.
The European Respiratory Journal
|
February 6, 2025
First assessment of photon-counting CT for virtual bronchoscopic navigation
Marcel Opitz, Faustina Funke, Kaid Darwiche, et al.
American Journal of Human Genetics
|
May 4, 2000
A gene for hypotrichosis simplex of the scalp maps to chromosome 6p21.3
R C Betz, Y A Lee, A Bygum, et al.
Page
of 29