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Whole exome sequencing reveals de novo pathogenic variants in KAT6A as a cause of a neurodevelopmental disorder.
Thrombopoietin Receptor Agonist Use in Children: Data From the Pediatric ITP Consortium of North America ICON2 Study.
Development of a sickle cell disease readiness for transition assessment.
Estimating the cost of delivering direct nutrition interventions at scale: national and subnational level insights from India.
Assessment and treatment of pain in thalassemia.
Elevations in serum anti-flagellin and anti-LPS Igs are related to growth faltering in young Tanzanian children.
The Contribution of the Corpus Callosum to Language Lateralization.
Community engagement to inform the development of a sickle cell counselor training and certification program in Ghana.
De Novo Mutations of RERE Cause a Genetic Syndrome with Features that Overlap Those Associated with Proximal 1p36 Deletions.
Loss of Iroquois homeobox transcription factors 3 and 5 in osteoblasts disrupts cranial mineralization.