Frontiers Case report: A preterm infant with rubinstein-taybi
Por um escritor misterioso
Last updated 24 janeiro 2025
PDF) Genetic heterogeneity in corpus callosum agenesis
Frontiers The effects of early combined training on the physical development of preterm infants with different gestational ages
Frontiers The effects of early combined training on the physical development of preterm infants with different gestational ages
Rubinstein–Taybi Syndrome in a Filipino Infant with a Novel CREBBP Gene Pathogenic Variant
A) sequence analysis of the genomic DNA of our rubinstein-taybi
Frontiers in Pediatrics
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 Syndromic forms of congenital hyperinsulinism
Low bone mineral density on DXA and slipped capital femoral epiphysis as rare presentation in a child with Rubinstein-Taybi syndrome
Frontiers in Pediatrics
Frontiers in Pediatrics
Lucja Bieleninik - Norce
Frontiers Case report: A preterm infant with rubinstein-taybi syndrome and Marmorata telangiectatica harboring a frameshift mutation in the CREBBP gene
rubinstein-taybi syndrome - List of Frontiers' open access articles
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