Mosaic CREBBP mutation causes overlapping clinical features of Rubinstein– Taybi and Filippi syndromes
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A Novel CREBBP in-Frame Deletion Variant in a Chinese Girl with
Figure 1 from Mutations in CKAP2L, the human homolog of the mouse
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Figure 1 from Mutations in CKAP2L, the human homolog of the mouse
A case with Rubinstein-Taybi syndrome: A novel frameshift mutation
Characterization of 14 novel deletions underlying Rubinstein–Taybi
High frequency of mosaic CREBBP deletions in Rubinstein–Taybi
Rubinstein–Taybi syndrome in diverse populations - Tekendo
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Figure 1 from Mutations in CKAP2L, the human homolog of the mouse
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