Rubinstein-Taybi Syndrome 1

A novel mutation c.4003 G>C in the CREBBP gene in an adult female with Rubinstein–Taybi syndrome presenting with subtle dysmorphic features - Li - 2010 - American Journal of Medical Genetics Part

Cureus, Whole-Exome Sequencing Identified a Novel DYRK1A Variant in a Patient With Intellectual Developmental Disorder, Autosomal Dominant 7

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

genereviews.org - GeneReviews® - NCBI Bookshelf

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

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

Legius Syndrome - an overview

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

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

Approach to inherited hypertrichosis: A brief review - Indian Journal of Dermatology, Venereology and Leprology