PDF) Rubinstein-Taybi syndrome in diverse populations

A novel mutation c.4003 G>C in the CREBBP gene in an adult female with Rubinstein–Taybi syndrome presenting with subtle dysmorphic features - Li - 2010 - American Journal of Medical Genetics Part

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

A mosaic maternal splice donor mutation in the EHMT1 gene leads to aberrant transcripts and to Kleefstra syndrome in the offspring

Mutations in SRCAP, Encoding SNF2-Related CREBBP Activator Protein, Cause Floating-Harbor Syndrome - ScienceDirect

Cornelia de Lange Syndrome - GeneReviews® - NCBI Bookshelf

Cockayne Syndrome: Most Up-to-Date Encyclopedia, News & Reviews

JCM, Free Full-Text

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

Identification of de novo EP300 and PLAU variants in a patient

Rubinstein-Taybi syndrome with agenesis of corpus callosum