Medicine & Life Sciences
Adenosine Triphosphate
Albinism
Alleles
Alveolar capillary dysplasia
ATP-Binding Cassette Transporters
Cerebellar Hypoplasia
CHARGE Syndrome
Child
Chromosomes, Human, Pair 16
Coloboma
DNA
Ehlers-Danlos Syndrome
Epigenomics
Epilepsy
Eukaryotic Initiation Factor-2
fibroblast growth factor 21
Fibroblasts
Genes
Haplotypes
Intellectual Disability
Interstitial Lung Diseases
Kabuki syndrome
Kleefstra Syndrome
Leukoencephalopathies
Lung
Lung Diseases
Lung Transplantation
Microcephaly with Simplified Gyral Pattern
Mutation
National Heart, Lung, and Blood Institute (U.S.)
National Institutes of Health (U.S.)
Neonatal progeroid syndrome
Neurodevelopmental Disorders
Newborn Infant
Newborn Respiratory Distress Syndrome
Persistent Fetal Circulation Syndrome
Phenotype
Pontocerebellar Hypoplasia
Population
Premature Infants
Protein C
Proteins
Pseudoacromegaly with Severe Insulin Resistance
Rare Diseases
Respiratory Insufficiency
Surface-Active Agents
Surfactant Dysfunction
Technology
Virulence
Whole Exome Sequencing
