Frontiers Case report: A preterm infant with rubinstein-taybi
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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
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Abstracts - 2023 - Congenital Anomalies - Wiley Online Library
A) sequence analysis of the genomic DNA of our 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
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Monash Health Research Report 2012
