Anaesthesia Management in a Child with Rubinstein - Taybi Syndrome

Rubinstein-Taybi Syndrome - GeneReviews® - NCBI Bookshelf

Figure 1. [Facial appearance of a girl age 11 years with FHS (SRCAP pathogenic variant p.Arg2444Ter)]. - GeneReviews® - NCBI Bookshelf

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

Cureus, Whole-Exome Sequencing Identified a Novel DYRK1A Variant in a Patient With Intellectual Developmental Disorder, Autosomal Dominant 7

Cornelia de Lange Syndrome - GeneReviews® - NCBI Bookshelf

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

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

Approach to inherited hypertrichosis: A brief review - Indian Journal of Dermatology, Venereology and Leprology

Rubinstein-Taybi syndrome with agenesis of corpus callosum