Forgotten Diseases Research Foundation

Rubinstein-Taybi Syndrome 2 disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials

PDF) Rubinstein-Taybi syndrome: Dental manifestations and management

Ocular symptoms in patients with Rubinstein-Taybi syndrome; 117 out of

Analysis of mutations within the intron20 splice donor site of CREBBP in patients with and without classical RSTS

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. - Document

Clinical and molecular findings of the six patients with Rubinstein

Case report: a Chinese girl like atypical Rubinstein–Taybi syndrome caused by a novel heterozygous mutation of the EP300 gene, BMC Medical Genomics

Rubinstein-Taybi Syndrome: A Rare Case Report

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Mosaic CREBBP mutation causes overlapping clinical features of