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Journal of Medical Genetics
|
December 10, 2002
Thrombocytopenia-absent radius syndrome: a clinical genetic study
K L Greenhalgh, R T Howell, A Bottani, et al.
Medicine and Science in Sports and Exercise
|
October 1, 1994
Physiological comparison of uphill roller skiing: diagonal stride versus double pole
M D Hoffman, P S Clifford, P B Watts, et al.
Plos One
|
December 15, 2015
The TGFβ1 Promoter SNP C-509T and Food Sensitization Promote Esophageal Remodeling in Pediatric Eosinophilic Esophagitis
Renee Rawson, Arjun Anilkumar, Robert O Newbury, et al.
Trials
|
June 21, 2014
Intervention to reduce excessive alcohol consumption and improve comorbidity outcomes in hypertensive or depressed primary care patients: two parallel cluster randomized feasibility trials
Graeme B Wilson, Catherine Wray, Ruth McGovern, et al.
American Journal of Human Genetics
|
December 1, 1996
A translocation at 12q2 refines the interval containing the Holt-Oram syndrome 1 gene
J A Terrett, R Newbury-Ecob, N M Smith, et al.
Psychological Medicine
|
September 25, 2020
Association between genetic and socioenvironmental risk for schizophrenia during upbringing in a UK longitudinal cohort
J B Newbury, L Arseneault, A Caspi, et al.
Metallurgical and Materials Transactions. A. Physical Metallurgy and Materials Science
|
October 16, 2020
Solidification of Ni-Re Peritectic Alloys
W J Boettinger, D E Newbury, N W M Ritchie, et al.
Plos One
|
November 6, 2009
Heat shock protein-derived T-cell epitopes contribute to autoimmune inflammation in pediatric Crohn's disease
Gisella L Puga Yung, Meredith Fidler, Erika Albani, et al.
Atmospheric Measurement Techniques
|
December 26, 2017
Intercomparison of Open-Path Trace Gas Measurements with Two Dual Frequency Comb Spectrometers
Eleanor M Waxman, Kevin C Cossel, Gar-Wing Truong, et al.
European Journal of Human Genetics : EJHG
|
April 5, 2012
Van Maldergem syndrome: further characterisation and evidence for neuronal migration abnormalities and autosomal recessive inheritance
Sahar Mansour, Marielle Swinkels, Paulien A Terhal, et al.
Page
of 83
Search research articles
Search
Showing results (601-610 of 826) with videos related to
Sort By:
Page
of 83
Journal of Medical Genetics
|
December 10, 2002
Thrombocytopenia-absent radius syndrome: a clinical genetic study
K L Greenhalgh, R T Howell, A Bottani, et al.
Medicine and Science in Sports and Exercise
|
October 1, 1994
Physiological comparison of uphill roller skiing: diagonal stride versus double pole
M D Hoffman, P S Clifford, P B Watts, et al.
Plos One
|
December 15, 2015
The TGFβ1 Promoter SNP C-509T and Food Sensitization Promote Esophageal Remodeling in Pediatric Eosinophilic Esophagitis
Renee Rawson, Arjun Anilkumar, Robert O Newbury, et al.
Trials
|
June 21, 2014
Intervention to reduce excessive alcohol consumption and improve comorbidity outcomes in hypertensive or depressed primary care patients: two parallel cluster randomized feasibility trials
Graeme B Wilson, Catherine Wray, Ruth McGovern, et al.
American Journal of Human Genetics
|
December 1, 1996
A translocation at 12q2 refines the interval containing the Holt-Oram syndrome 1 gene
J A Terrett, R Newbury-Ecob, N M Smith, et al.
Psychological Medicine
|
September 25, 2020
Association between genetic and socioenvironmental risk for schizophrenia during upbringing in a UK longitudinal cohort
J B Newbury, L Arseneault, A Caspi, et al.
Metallurgical and Materials Transactions. A. Physical Metallurgy and Materials Science
|
October 16, 2020
Solidification of Ni-Re Peritectic Alloys
W J Boettinger, D E Newbury, N W M Ritchie, et al.
Plos One
|
November 6, 2009
Heat shock protein-derived T-cell epitopes contribute to autoimmune inflammation in pediatric Crohn's disease
Gisella L Puga Yung, Meredith Fidler, Erika Albani, et al.
Atmospheric Measurement Techniques
|
December 26, 2017
Intercomparison of Open-Path Trace Gas Measurements with Two Dual Frequency Comb Spectrometers
Eleanor M Waxman, Kevin C Cossel, Gar-Wing Truong, et al.
European Journal of Human Genetics : EJHG
|
April 5, 2012
Van Maldergem syndrome: further characterisation and evidence for neuronal migration abnormalities and autosomal recessive inheritance
Sahar Mansour, Marielle Swinkels, Paulien A Terhal, et al.
Page
of 83