Keyphrases
Cyanotic Newborn
100%
Cyanosis
100%
Cyanotic Congenital Heart Disease
50%
Left Ventricular Noncompaction
50%
Part 2A
50%
High-sensitivity Troponin T
50%
Hemodynamically Significant Patent Ductus Arteriosus
50%
Gain-of-function mutation
50%
Neonatologist
50%
Congenital Heart Defects
50%
Cardiologists
50%
Preterm Infants
50%
Intellectual Disability
37%
N-terminal Pro-brain Natriuretic Peptide (NT-proBNP)
35%
Hemoglobin
30%
Hyperoxia Test
25%
Initial Management
25%
Prostaglandin E1 (PGE1)
25%
Pulse Oximetry
25%
Chest Radiography
25%
Cardiac Echocardiography
25%
Heart Disease
25%
Congenital Heart Disease
25%
High Index of Suspicion
25%
Congenital Lesions
25%
Lifesaving
25%
Appropriate Management
25%
Pathophysiology
25%
Ductal Dependent
25%
Developmental Delay
25%
Echocardiogram
14%
Global Developmental Delay
12%
CNV Analysis
12%
Stochastic Factors
12%
Congenital Brain Anomalies
12%
Small Families
12%
Relative Macrocephaly
12%
Exome Sequencing
12%
Dysmorphic Features
12%
Cardiac Transplantation
12%
DNA Repair
12%
Penetrance
12%
Human Subjects
12%
Single-gene Deletion
12%
RNA Binding
12%
Phenotypic Outcome
12%
Octamer
12%
RNA Synthesis
12%
Atrial Septal Defect
12%
Male Infant
12%
Medicine and Dentistry
Cyanosis
100%
Neonatal Infant
100%
Troponin T
50%
Noncompaction Cardiomyopathy
50%
Cyanotic Heart Defect
50%
Patent Ductus Arteriosus
50%
Congenital Heart Defect
50%
Echocardiography
39%
Developmental Delay
37%
Persistent Truncus Arteriosus
35%
Pulse Oximetry
35%
Thorax Radiography
25%
Diagnosis
25%
Infusion
25%
Prostaglandin E1
25%
Heart Disease
25%
Hyperoxia
25%
Pathophysiology
25%
Physical Examination
25%
Heart Injury
25%
Corpus Callosum
12%
Brain Malformation
12%
Dysmorphic Feature
12%
DNA RNA Hybridization
12%
Gene Deletion
12%
DNA Binding Protein
12%
Macrocephaly
12%
Human Subject
12%
Atrial Septal Defect
12%
Ventricular Septal Defect
12%
DNA Repair
12%
RNA Synthesis
12%
Exome Sequencing
12%
Penetrance
12%
RNA Binding
12%
Brain Imaging
12%
Heart Transplantation
12%
Myocardial Disease
12%
Newborn Period
10%
Embryonic Hemoglobin
10%
Heart Function
7%
Chromosome Aberration
7%
Pregnancy
7%
Student T Test
7%
Congenital Malformation
7%
Birth Weight
7%
Biochemistry, Genetics and Molecular Biology
Intellectual Disability
50%
Troponin T
50%
Epigenetics
16%
Exome Sequencing
16%
DNA Repair
16%
DNA RNA Hybridization
16%
Genetics
16%
RNA Synthesis
16%
POU Domain
16%
RNA Binding
16%
Human
16%
Penetrance
16%
Gene Deletion
16%
DNA-binding Protein
16%
Birth Weight
7%
Pregnancy
7%
Heart Function
7%
Student's t-Test
7%
Chromosomal Disorder
7%
