Subclass IgG levels of patients with Rubinstein-Taybi syndrome compared

Rubinstein-Taybi syndrome: MedlinePlus Genetics

PDF) Rubinstein-Taybi syndrome: Dental manifestations and management

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

Rubinstein-Taybi Syndrome

PDF) Prevalence of Immunological Defects in a Cohort of 97 Rubinstein–Taybi Syndrome Patients

PDF) Identification of a novel de novo mutation of CREBBP in a patient with Rubinstein-Taybi syndrome by targeted next-generation sequencing: A case report

Rubinstein-Taybi Syndrome: A Rare Case Report

Rubinstein-Taybi 2 associated to novel EP300 mutations: deepening the clinical and genetic spectrum, BMC Medical Genetics

Expanding the phenotype associated to KMT2A variants: overlapping