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Molecular Cytogenetics
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June 11, 2015
Language impairment in a case of a complex chromosomal rearrangement with a breakpoint downstream of FOXP2
Daniela Moralli, Ron Nudel, May T M Chan, et al.
Cancer Research
|
January 13, 2001
Genetic heterogeneity in familial juvenile polyposis
S C Huang, C R Chen, J E Lavine, et al.
Nutrition & Diabetes
|
November 17, 2012
Proximal correlates of metabolic phenotypes during 'at-risk' and 'case' stages of the metabolic disease continuum
M T Haren, G Misan, J F Grant, et al.
Optics Express
|
June 11, 2024
Validation of open-path dual-comb spectroscopy against an O<sub>2</sub> background: erratum
Nathan A Malarich, Brian R Washburn, Kevin C Cossel, et al.
Mucosal Immunology
|
October 23, 2019
TGFβ1 single-nucleotide polymorphism C-509T alters mucosal cell function in pediatric eosinophilic esophagitis
L D Duong, R Rawson, A Bezryadina, et al.
European Journal of Epidemiology
|
January 7, 2023
Research-ready data: the C-Surv data model
Sarah Bauermeister, Joshua R Bauermeister, Ruth Bridgman, et al.
Biological Psychiatry
|
April 5, 2011
DCDC2, KIAA0319 and CMIP are associated with reading-related traits
Tom S Scerri, Andrew P Morris, Lyn-Louise Buckingham, et al.
American Journal of Human Genetics
|
August 9, 2011
Exome sequencing identifies a DYNC1H1 mutation in a large pedigree with dominant axonal Charcot-Marie-Tooth disease
Michael N Weedon, Robert Hastings, Richard Caswell, et al.
Optics Express
|
January 7, 2017
Accurate frequency referencing for fieldable dual-comb spectroscopy
Gar-Wing Truong, Eleanor M Waxman, Kevin C Cossel, et al.
Optics Letters
|
May 4, 2005
Stabilized frequency comb with a self-referenced femtosecond Cr:forsterite laser
K Kim, B R Washburn, G Wilpers, et al.
Page
of 83
Search research articles
Search
Showing results (551-560 of 826) with videos related to
Sort By:
Page
of 83
Molecular Cytogenetics
|
June 11, 2015
Language impairment in a case of a complex chromosomal rearrangement with a breakpoint downstream of FOXP2
Daniela Moralli, Ron Nudel, May T M Chan, et al.
Cancer Research
|
January 13, 2001
Genetic heterogeneity in familial juvenile polyposis
S C Huang, C R Chen, J E Lavine, et al.
Nutrition & Diabetes
|
November 17, 2012
Proximal correlates of metabolic phenotypes during 'at-risk' and 'case' stages of the metabolic disease continuum
M T Haren, G Misan, J F Grant, et al.
Optics Express
|
June 11, 2024
Validation of open-path dual-comb spectroscopy against an O<sub>2</sub> background: erratum
Nathan A Malarich, Brian R Washburn, Kevin C Cossel, et al.
Mucosal Immunology
|
October 23, 2019
TGFβ1 single-nucleotide polymorphism C-509T alters mucosal cell function in pediatric eosinophilic esophagitis
L D Duong, R Rawson, A Bezryadina, et al.
European Journal of Epidemiology
|
January 7, 2023
Research-ready data: the C-Surv data model
Sarah Bauermeister, Joshua R Bauermeister, Ruth Bridgman, et al.
Biological Psychiatry
|
April 5, 2011
DCDC2, KIAA0319 and CMIP are associated with reading-related traits
Tom S Scerri, Andrew P Morris, Lyn-Louise Buckingham, et al.
American Journal of Human Genetics
|
August 9, 2011
Exome sequencing identifies a DYNC1H1 mutation in a large pedigree with dominant axonal Charcot-Marie-Tooth disease
Michael N Weedon, Robert Hastings, Richard Caswell, et al.
Optics Express
|
January 7, 2017
Accurate frequency referencing for fieldable dual-comb spectroscopy
Gar-Wing Truong, Eleanor M Waxman, Kevin C Cossel, et al.
Optics Letters
|
May 4, 2005
Stabilized frequency comb with a self-referenced femtosecond Cr:forsterite laser
K Kim, B R Washburn, G Wilpers, et al.
Page
of 83