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Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
January 25, 2020
Exome sequencing in newborns with congenital deafness as a model for genomic newborn screening: the Baby Beyond Hearing project
Lilian Downie, Jane Halliday, Sharon Lewis, et al.
American Journal of Human Genetics
|
May 29, 2025
Public preferences for the value and implementation of genomic newborn screening: Insights from two discrete choice experiments in Australia
Riccarda Peters, Stephanie Best, Fiona Lynch, et al.
Clinical Case Reports
|
January 2, 2020
Whole exome sequencing reveals a de novo missense variant in <i>EEF1A2</i> in a Rett syndrome-like patient
Simranpreet Kaur, Nicole J Van Bergen, Wendy Anne Gold, et al.
Molecular Syndromology
|
April 8, 2020
Rapid Identification of Biallelic <i>SPTB</i> Mutation in a Neonate with Severe Congenital Hemolytic Anemia and Liver Failure
Christopher M Richmond, Sally Campbell, Hee W Foo, et al.
European Journal of Human Genetics : EJHG
|
February 26, 2026
Mainstreaming genomic testing for mitochondrial disease in Australia
Megan Ball, Naomi Baker, Sze Chern Lim, et al.
Genomics
|
May 4, 2013
Exploring the utility of human DNA methylation arrays for profiling mouse genomic DNA
Nicholas C Wong, Jane Ng, Nathan E Hall, et al.
Plos One
|
February 25, 2012
Role of histone acetylation in the stimulatory effect of valproic acid on vascular endothelial tissue-type plasminogen activator expression
Pia Larsson, Erik Ulfhammer, Mia Magnusson, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
February 19, 2022
Is faster better? An economic evaluation of rapid and ultra-rapid genomic testing in critically ill infants and children
Ilias Goranitis, You Wu, Sebastian Lunke, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
August 31, 2018
Correction: Does genomic sequencing early in the diagnostic trajectory make a difference? A follow-up study of clinical outcomes and cost-effectiveness
Zornitza Stark, Deborah Schofield, Melissa Martyn, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 17, 2018
Does genomic sequencing early in the diagnostic trajectory make a difference? A follow-up study of clinical outcomes and cost-effectiveness
Zornitza Stark, Deborah Schofield, Melissa Martyn, et al.
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of 12
Search research articles
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Showing results (21-30 of 117) with videos related to
Sort By:
Page
of 12
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
January 25, 2020
Exome sequencing in newborns with congenital deafness as a model for genomic newborn screening: the Baby Beyond Hearing project
Lilian Downie, Jane Halliday, Sharon Lewis, et al.
American Journal of Human Genetics
|
May 29, 2025
Public preferences for the value and implementation of genomic newborn screening: Insights from two discrete choice experiments in Australia
Riccarda Peters, Stephanie Best, Fiona Lynch, et al.
Clinical Case Reports
|
January 2, 2020
Whole exome sequencing reveals a de novo missense variant in <i>EEF1A2</i> in a Rett syndrome-like patient
Simranpreet Kaur, Nicole J Van Bergen, Wendy Anne Gold, et al.
Molecular Syndromology
|
April 8, 2020
Rapid Identification of Biallelic <i>SPTB</i> Mutation in a Neonate with Severe Congenital Hemolytic Anemia and Liver Failure
Christopher M Richmond, Sally Campbell, Hee W Foo, et al.
European Journal of Human Genetics : EJHG
|
February 26, 2026
Mainstreaming genomic testing for mitochondrial disease in Australia
Megan Ball, Naomi Baker, Sze Chern Lim, et al.
Genomics
|
May 4, 2013
Exploring the utility of human DNA methylation arrays for profiling mouse genomic DNA
Nicholas C Wong, Jane Ng, Nathan E Hall, et al.
Plos One
|
February 25, 2012
Role of histone acetylation in the stimulatory effect of valproic acid on vascular endothelial tissue-type plasminogen activator expression
Pia Larsson, Erik Ulfhammer, Mia Magnusson, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
February 19, 2022
Is faster better? An economic evaluation of rapid and ultra-rapid genomic testing in critically ill infants and children
Ilias Goranitis, You Wu, Sebastian Lunke, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
August 31, 2018
Correction: Does genomic sequencing early in the diagnostic trajectory make a difference? A follow-up study of clinical outcomes and cost-effectiveness
Zornitza Stark, Deborah Schofield, Melissa Martyn, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 17, 2018
Does genomic sequencing early in the diagnostic trajectory make a difference? A follow-up study of clinical outcomes and cost-effectiveness
Zornitza Stark, Deborah Schofield, Melissa Martyn, et al.
Page
of 12