Frontiers Case report: A preterm infant with rubinstein-taybi

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Last updated 22 março 2025
Frontiers  Case report: A preterm infant with rubinstein-taybi
Frontiers  Case report: A preterm infant with rubinstein-taybi
PDF] Chromosome 16p13.3 Contiguous Gene Deletion Syndrome including the SLX4, DNASE1, TRAP1, and CREBBP Genes Presenting as a Relatively Mild Rubinstein–Taybi Syndrome Phenotype: A Case Report of a Saudi Boy
Frontiers  Case report: A preterm infant with rubinstein-taybi
novel frameshift mutation - List of Frontiers' open access articles
Frontiers  Case report: A preterm infant with rubinstein-taybi
Abstracts - 2023 - Congenital Anomalies - Wiley Online Library
Frontiers  Case report: A preterm infant with rubinstein-taybi
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Frontiers  Case report: A preterm infant with rubinstein-taybi
Rubinstein-Taybi Syndrome: A Pediatric Case Report
Frontiers  Case report: A preterm infant with rubinstein-taybi
Frontiers in Pediatrics
Frontiers  Case report: A preterm infant with rubinstein-taybi
rubinstein-taybi syndrome - List of Frontiers' open access articles
Frontiers  Case report: A preterm infant with rubinstein-taybi
Frontiers in Pediatrics
Frontiers  Case report: A preterm infant with rubinstein-taybi
Patent Ductus Arteriosus: A Contemporary Perspective for the Pediatric and Adult Cardiac Care Provider
Frontiers  Case report: A preterm infant with rubinstein-taybi
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