Rubinstein-Taybi syndrome: principal oral and dental disorders and

Rubinstein-Taybi Syndrome

Rubinstein-Taybi Syndrome - GeneReviews® - NCBI Bookshelf

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

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

The novel and recurrent variants in exon 31 of CREBBP in Japanese patients with Menke–Hennekam syndrome - Nishi - 2022 - American Journal of Medical Genetics Part A - Wiley Online Library

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

JCM, Free Full-Text

NRF1 Association with AUTS2-Polycomb Mediates Specific Gene Activation in the Brain

What is CdLS? Ben and his Brothers: Life with 4 boys and CdLS

(PDF) Identification of de novo EP300 and PLAU variants in a