Subclass IgG levels of patients with Rubinstein-Taybi syndrome compared

Rubinstein-Taybi Syndrome OMIM# 180849 - FDNA™

Congenital glaucoma as a presenting feature of Rubinstein-Taybi

PDF) Rubinstein-Taybi syndrome: Dental manifestations and management

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

PDF) FISH studies in 45 patients with Rubinstein-Taybi syndrome: Deletions associated with polysplenia, hypoplastic left heart and death in infancy

Two adults with Rubinstein–Taybi syndrome with mild mental retardation, glaucoma, normal growth and skull circumference, and camptodactyly of third fingers - Wieczorek - 2009 - American Journal of Medical Genetics Part A

Genes involved in histone acetylation known to cause rare diseases

IJMS, Free Full-Text

Genetic heterogeneity in Rubinstein–Taybi syndrome: delineation of the phenotype of the first patients carrying mutations in EP300

Expanding the phenotype associated to KMT2A variants: overlapping clinical signs between Wiedemann–Steiner and Rubinstein–Taybi syndromes