Rubinstein-Taybi syndrome (RTS)

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Rubinstein-Taybi Syndrome 1

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

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

PDF) Rubinstein-Taybi syndrome: Dental manifestations and management

Floating-Harbor syndrome: MedlinePlus Genetics

PDF) Rubinstein-Taybi syndrome in diverse populations

Rubinstein–Taybi syndrome in diverse populations - Tekendo‐Ngongang - 2020 - American Journal of Medical Genetics Part A - Wiley Online Library

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

Expanding the phenotype associated to KMT2A variants: overlapping