PDF) Rubinstein-Taybi syndrome in diverse populations

Rubinstein-Taybi Syndrome - GeneReviews® - NCBI Bookshelf

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

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

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

Clinical heterogeneity of Kabuki syndrome in a cohort of Italian patients and review of the literature

PDF) An unusual presentation of Rubinstein-Taybi Syndrome with bilateral postaxial polydactyly Corresponding author

Beckwith-Wiedemann Syndrome - GeneReviews® - NCBI Bookshelf

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

A novel CREBBP mutation and its phenotype in a case of Rubinstein–Taybi syndrome, BMC Medical Genomics

Rubinstein-Taybi syndrome: principal oral and dental disorders and literature update