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Publications by F. Sessions Cole
De Novo Variants in WDR37 Are Associated With Epilepsy, Colobomas, Dysmorphism, Developmental Delay, Intellectual Disability, and Cerebellar Hypoplasia
American Journal of Human Genetics
Genetics
Heterogeneous Pulmonary Phenotypes Associated With Mutations in the Thyroid Transcription Factor Gene NKX2-1
Chest
Cardiology
Critical Care
Cardiovascular Medicine
Intensive Care Medicine
Pulmonary
Respiratory Medicine
Functional Assays to Screen and Dissect Genomic Hits
Circulation. Genomic and precision medicine
Genetics
Cardiovascular Medicine
Cardiology
Synonymous ABCA3 Variants Do Not Increase Risk for Neonatal Respiratory Distress Syndrome
Journal of Pediatrics
Child Health
Pediatrics
Perinatology
Genetic Factors Contribute to Risk for Neonatal Respiratory Distress Syndrome Among Moderately Preterm, Late Preterm, and Term Infants
Journal of Pediatrics
Child Health
Pediatrics
Perinatology
Functional Characterization of Biallelic RTTN Variants Identified in an Infant With Microcephaly, Simplified Gyral Pattern, Pontocerebellar Hypoplasia, and Seizures
Pediatric Research
Child Health
Pediatrics
Perinatology
Congenital Lymphocytic Choriomeningitis Virus
Journal of Child Neurology
Child Health
Neurology
Pediatrics
Perinatology
Cloning the Gene for an Inherited Human Disorder—chronic Granulomatous Disease—on the Basis of Its Chromosomal Location
Nature
Multidisciplinary
Surfactant Protein B: Unambiguously Necessary for Adult Pulmonary Function
American Journal of Physiology - Lung Cellular and Molecular Physiology
Pulmonary
Respiratory Medicine
Physiology
Cell Biology
Inherited Surfactant Deficiency Caused by Uniparental Disomy of Rare Mutations in the Surfactant Protein-B and ATP Binding Cassette, Subfamily A, Member 3 Genes
Journal of Pediatrics
Child Health
Pediatrics
Perinatology
