about
Modeling congenital disease and inborn errors of development in Drosophila melanogasterApplicability of digital PCR to the investigation of pediatric-onset genetic disordersSudden Unexpected Death in Fetal Life Through Early ChildhoodA novel 33-Gene targeted resequencing panel provides accurate, clinical-grade diagnosis and improves patient management for rare inherited anaemiasCancer diagnostics: The journey from histomorphology to molecular profiling.NGS Technologies as a Turning Point in Rare Disease Research , Diagnosis and Treatment.Implementing genomics and pharmacogenomics in the clinic: The National Human Genome Research Institute's genomic medicine portfolio.Clinical Versus Research Sequencing.The clinical utility of next-generation sequencing in the neonatal intensive care unitMendeliome sequencing enables differential diagnosis and treatment of neonatal lactic acidosis.Intersociety policy statement on the use of whole-exome sequencing in the critically ill newborn infant.Genomic Disorders in Psychiatry-What Does the Clinician Need to Know?Diagnostic Impact and Cost-effectiveness of Whole-Exome Sequencing for Ambulant Children With Suspected Monogenic Conditions.Pediatric Palliative Care in Infants and Neonates.Sudden infant death syndrome and inherited cardiac conditions.Rapid whole-genome sequencing decreases infant morbidity and cost of hospitalization.The BabySeq project: implementing genomic sequencing in newborns
P2860
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P2860
description
2015 nî lūn-bûn
@nan
2015年の論文
@ja
2015年学术文章
@wuu
2015年学术文章
@zh-cn
2015年学术文章
@zh-hans
2015年学术文章
@zh-my
2015年学术文章
@zh-sg
2015年學術文章
@yue
2015年學術文章
@zh
2015年學術文章
@zh-hant
name
Rapid whole genome sequencing and precision neonatology
@ast
Rapid whole genome sequencing and precision neonatology
@en
type
label
Rapid whole genome sequencing and precision neonatology
@ast
Rapid whole genome sequencing and precision neonatology
@en
prefLabel
Rapid whole genome sequencing and precision neonatology
@ast
Rapid whole genome sequencing and precision neonatology
@en
P2860
P1476
Rapid whole genome sequencing and precision neonatology
@en
P2093
Joshua E Petrikin
Laurie D Smith
P2860
P304
P356
10.1053/J.SEMPERI.2015.09.009
P577
2015-10-28T00:00:00Z