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

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

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

Extending the clinical and genetic spectrum of ARID2 related intellectual disability. A case series of 7 patients - ScienceDirect

PDF) Rubinstein-Taybi syndrome in diverse populations

Müllerian Agenesis in a patient with Rubinstein-Taybi Syndrome: A Case Series and Review of the Overlapping Developmental Biologic Pathways - Journal of Pediatric and Adolescent Gynecology

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

A novel CREBBP mutation and its phenotype in a case of Rubinstein

Rubinstein-Taybi syndrome with agenesis of corpus callosum. - Abstract - Europe PMC

Frontiers Behavioral and neuropsychiatric challenges across the lifespan in individuals with Rubinstein-Taybi syndrome