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Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
April 16, 2009
Expanded newborn screening in Texas: a survey and educational module addressing the knowledge of pediatric residents
Amy Stanford Wells, Hope Northrup, Sharon S Crandell, et al.
Gene
|
June 13, 2023
Mild TSC phenotype and non-penetrance associated with a frameshift variant in TSC2 prompts caution in evaluating pathogenicity of frameshift variants
Laura S Farach, Hope Northrup, Mark Nellist, et al.
Maternal and Child Health Journal
|
January 6, 2019
Psychological Flexibility and Depression in New Mothers of Medically Vulnerable Infants: A Mediational Analysis
Angela L Stotts, Yolanda R Villarreal, Michelle R Klawans, et al.
American Journal of Perinatology
|
August 12, 2014
Randomized, controlled pilot trial of bupropion for pregnant smokers: challenges and future directions
Angela L Stotts, Thomas F Northrup, Paul M Cinciripini, et al.
Journal of Veterinary Internal Medicine
|
May 31, 2001
Retrospective study of orthovoltage radiation therapy for nasal tumors in 42 dogs
N C Northrup, S M Etue, D M Ruslander, et al.
Nature Materials
|
November 10, 2009
Large modulation of carrier transport by grain-boundary molecular packing and microstructure in organic thin films
Jonathan Rivnay, Leslie H Jimison, John E Northrup, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 11, 2013
Self-reported reproductive health in women with tuberous sclerosis complex
Emily K Gabitzsch, Syed S Hashmi, Mary Kay Koenig, et al.
Plos One
|
December 11, 2012
Folate metabolism gene 5,10-methylenetetrahydrofolate reductase (MTHFR) is associated with ADHD in myelomeningocele patients
Catherine J Spellicy, Hope Northrup, Jack M Fletcher, et al.
Pediatric Neurology
|
October 27, 2015
Clinical Electroencephalographic Biomarker for Impending Epilepsy in Asymptomatic Tuberous Sclerosis Complex Infants
Joyce Y Wu, Jurriaan M Peters, Monisha Goyal, et al.
Plos One
|
September 24, 2020
Burden of rare deleterious variants in WNT signaling genes among 511 myelomeningocele patients
Luke Hebert, Paul Hillman, Craig Baker, et al.
Page
of 81
Search research articles
Search
Showing results (531-540 of 803) with videos related to
Sort By:
Page
of 81
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
April 16, 2009
Expanded newborn screening in Texas: a survey and educational module addressing the knowledge of pediatric residents
Amy Stanford Wells, Hope Northrup, Sharon S Crandell, et al.
Gene
|
June 13, 2023
Mild TSC phenotype and non-penetrance associated with a frameshift variant in TSC2 prompts caution in evaluating pathogenicity of frameshift variants
Laura S Farach, Hope Northrup, Mark Nellist, et al.
Maternal and Child Health Journal
|
January 6, 2019
Psychological Flexibility and Depression in New Mothers of Medically Vulnerable Infants: A Mediational Analysis
Angela L Stotts, Yolanda R Villarreal, Michelle R Klawans, et al.
American Journal of Perinatology
|
August 12, 2014
Randomized, controlled pilot trial of bupropion for pregnant smokers: challenges and future directions
Angela L Stotts, Thomas F Northrup, Paul M Cinciripini, et al.
Journal of Veterinary Internal Medicine
|
May 31, 2001
Retrospective study of orthovoltage radiation therapy for nasal tumors in 42 dogs
N C Northrup, S M Etue, D M Ruslander, et al.
Nature Materials
|
November 10, 2009
Large modulation of carrier transport by grain-boundary molecular packing and microstructure in organic thin films
Jonathan Rivnay, Leslie H Jimison, John E Northrup, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 11, 2013
Self-reported reproductive health in women with tuberous sclerosis complex
Emily K Gabitzsch, Syed S Hashmi, Mary Kay Koenig, et al.
Plos One
|
December 11, 2012
Folate metabolism gene 5,10-methylenetetrahydrofolate reductase (MTHFR) is associated with ADHD in myelomeningocele patients
Catherine J Spellicy, Hope Northrup, Jack M Fletcher, et al.
Pediatric Neurology
|
October 27, 2015
Clinical Electroencephalographic Biomarker for Impending Epilepsy in Asymptomatic Tuberous Sclerosis Complex Infants
Joyce Y Wu, Jurriaan M Peters, Monisha Goyal, et al.
Plos One
|
September 24, 2020
Burden of rare deleterious variants in WNT signaling genes among 511 myelomeningocele patients
Luke Hebert, Paul Hillman, Craig Baker, et al.
Page
of 81