Add to ORKGIn newborn intensive care units (NICUs), the science and art of prognostication often have life and ...
Rapid genomic sequencing (RGS) is increasingly being used in the care of critically ill children. He...
The advancements made in next‐generation sequencing (NGS) technology over the past two decades have ...
The second Newborn Sequencing in Genomic Medicine and Public Health (NSIGHT2) study was a randomized...
Diagnostic genome-wide sequencing (exome or genome sequencing and data analysis for high-penetrance ...
Traditionally, genetic testing has been too slow or perceived to be impractical to initial managemen...
Purpose: Several studies have reported diagnostic yields up to 57% for rapid exome or genome sequenc...
Rapid genome sequencing in critically ill infants is increasingly identified as a crucial test for p...
Understanding causes of infant mortality shapes public health policy and prioritizes diseases for in...
OBJECTIVES:Genetic disorders are a leading contributor to mortality in the neonatal ICU and PICU in ...
The second Newborn Sequencing in Genomic Medicine and Public Health study was a randomized, controll...
© 2021 Fiona Jacqueline LynchGenomic technologies are showing great promise in the neonatal and paed...
Newborn screening (NBS) dramatically improves outcomes in severe childhood disorders by treatment be...
Introduction: Undiagnosed genetic diseases are one of the leading causes of infant morbidity and mo...
International audienceObtaining a rapid etiological diagnosis for infants with early-onset rare dise...
In newborn intensive care units (NICUs), the science and art of prognostication often have life and ...
Rapid genomic sequencing (RGS) is increasingly being used in the care of critically ill children. He...
The advancements made in next‐generation sequencing (NGS) technology over the past two decades have ...
The second Newborn Sequencing in Genomic Medicine and Public Health (NSIGHT2) study was a randomized...
Diagnostic genome-wide sequencing (exome or genome sequencing and data analysis for high-penetrance ...
Traditionally, genetic testing has been too slow or perceived to be impractical to initial managemen...
Purpose: Several studies have reported diagnostic yields up to 57% for rapid exome or genome sequenc...
Rapid genome sequencing in critically ill infants is increasingly identified as a crucial test for p...
Understanding causes of infant mortality shapes public health policy and prioritizes diseases for in...
OBJECTIVES:Genetic disorders are a leading contributor to mortality in the neonatal ICU and PICU in ...
The second Newborn Sequencing in Genomic Medicine and Public Health study was a randomized, controll...
© 2021 Fiona Jacqueline LynchGenomic technologies are showing great promise in the neonatal and paed...
Newborn screening (NBS) dramatically improves outcomes in severe childhood disorders by treatment be...
Introduction: Undiagnosed genetic diseases are one of the leading causes of infant morbidity and mo...
International audienceObtaining a rapid etiological diagnosis for infants with early-onset rare dise...
In newborn intensive care units (NICUs), the science and art of prognostication often have life and ...
Rapid genomic sequencing (RGS) is increasingly being used in the care of critically ill children. He...
The advancements made in next‐generation sequencing (NGS) technology over the past two decades have ...