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

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Rubinstein-Taybi Syndrome

Figure 2. [Broad terminal phalanges (A) and broad, radially deviated thumbs (B)]. - GeneReviews® - NCBI Bookshelf

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

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

PDF) Rubinstein-Taybi syndrome in diverse populations

Rubinstein-Taybi syndrome (RTS)

Beckwith-Wiedemann Syndrome - GeneReviews® - NCBI Bookshelf

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

Frontiers Behavioral and neuropsychiatric challenges across the