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Rubinstein-Taybi Syndrome: A Complete Overview — DermNet

Rubinstein-Taybi Syndrome

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

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

Floating-Harbor syndrome: MedlinePlus Genetics

PDF) Rubinstein-Taybi syndrome in diverse populations

JCM, Free Full-Text

Somatic and germ‐line mosaicism in Rubinstein–Taybi syndrome - Chiang - 2009 - American Journal of Medical Genetics Part A - Wiley Online Library

Expanding the phenotype associated to KMT2A variants: overlapping

Rubinstein-Taybi syndrome: principal oral and dental disorders and