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Rubinstein-Taybi syndrome: MedlinePlus Genetics

Characterization of 14 novel deletions underlying Rubinstein–Taybi syndrome: an update of the CREBBP deletion repertoire

PDF) Oro-dental features as useful diagnostic tool in Rubinstein–Taybi syndrome

OMIM diseases as a function of associated HPO phenotypes. Data include

Clinical and molecular findings of the six patients with Rubinstein

Rubinstein–Taybi syndrome associated with Chiari type I malformation caused by a large 16p13.3 microdeletion: A contiguous gene syndrome? - Wójcik - 2010 - American Journal of Medical Genetics Part A - Wiley Online Library

IJMS, Free Full-Text

Main clinical findings of the 16 Brazilian patients with

Mosaic CREBBP mutation causes overlapping clinical features of

Rubinstein-Taybi syndrome: clinical features, genetic basis