Mosaic CREBBP mutation causes overlapping clinical features of Rubinstein– Taybi and Filippi syndromes

PDF] Multiple Dental and Skeletal Abnormalities in an Individual

Further delineation of an entity caused by CREBBP and EP300

Mosaic CREBBP mutation causes overlapping clinical features of

Figure 1 from Mutations in CKAP2L, the human homolog of the mouse

Rubinstein-Taybi Syndrome: spectrum of CREBBP mutations in Italian

High frequency of mosaic CREBBP deletions in Rubinstein–Taybi

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Molecular studies in 10 cases of Rubinstein-Taybi syndrome

Frontiers Genetic Diagnosis of Rubinstein–Taybi Syndrome With

Characterization of 14 novel deletions underlying Rubinstein–Taybi

Microdeletions and mutations of CREBBP (CBP) gene can cause