Frontiers Case report: A preterm infant with rubinstein-taybi
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Frontiers in Pediatrics
Frontiers Case report: A preterm infant with rubinstein-taybi syndrome and Marmorata telangiectatica harboring a frameshift mutation in the CREBBP gene
PDF) Genetic heterogeneity in corpus callosum agenesis
rubinstein-taybi syndrome - List of Frontiers' open access articles
Frontiers Case report: A preterm infant with rubinstein-taybi syndrome and Marmorata telangiectatica harboring a 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
novel frameshift mutation - List of Frontiers' open access articles
Rubinstein-Taybi Syndrome: A Case Report
Frontiers Case Report: Treatment of Extremely Preterm Infants With Birthweight Below 300 g: Case Series
Frontiers in Pediatrics
Low bone mineral density on DXA and slipped capital femoral epiphysis as rare presentation in a child with Rubinstein-Taybi syndrome
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