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UCSF School of Medicine | Department of Pediatrics UCSF Medical Center

Whole exome sequencing reveals de novo pathogenic variants in KAT6A as a cause of a neurodevelopmental disorder.

  • Read more about 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.

  • Read more about 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.

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Estimating the cost of delivering direct nutrition interventions at scale: national and subnational level insights from India.

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Assessment and treatment of pain in thalassemia.

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Elevations in serum anti-flagellin and anti-LPS Igs are related to growth faltering in young Tanzanian children.

  • Read more about 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.

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Community engagement to inform the development of a sickle cell counselor training and certification program in Ghana.

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De Novo Mutations of RERE Cause a Genetic Syndrome with Features that Overlap Those Associated with Proximal 1p36 Deletions.

  • Read more about 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.

  • Read more about Loss of Iroquois homeobox transcription factors 3 and 5 in osteoblasts disrupts cranial mineralization.

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