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Rubinstein-Taybi Syndrome - GeneReviews® - NCBI Bookshelf

Rubinstein Taybi syndrome causes, symptoms, diagnosis, treatment & prognosis

Figure 2. [Dorsal (A) and palmar (B)]. - GeneReviews® - NCBI Bookshelf

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

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

PDF) The behavioral phenotype of Rubinstein–Taybi syndrome: A scoping review of the literature

Beckwith-Wiedemann Syndrome - GeneReviews® - NCBI Bookshelf

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

Rubinstein-Taybi syndrome: principal oral and dental disorders and