Frontiers Case report: A preterm infant with rubinstein-taybi
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Rubinstein–Taybi Syndrome in a Filipino Infant with a Novel CREBBP Gene Pathogenic Variant
Low bone mineral density on DXA and slipped capital femoral epiphysis as rare presentation in a child with Rubinstein-Taybi syndrome
novel frameshift mutation - List of Frontiers' open access articles
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 in Pediatrics
Frontiers Tailored treatments in inborn errors of immunity associated with atopy (IEIs-A) with skin involvement
A case with Rubinstein-Taybi syndrome: A novel frameshift mutation in the CREBBP gene.
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
rubinstein-taybi syndrome - List of Frontiers' open access articles
Patent Ductus Arteriosus: A Contemporary Perspective for the Pediatric and Adult Cardiac Care Provider
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