Mosaic CREBBP mutation causes overlapping clinical features of Rubinstein– Taybi and Filippi syndromes
Por um escritor misterioso
Last updated 17 novembro 2024
Figure 1 from Mutations in CKAP2L, the human homolog of the mouse
Hands showing syndactyly of fingers.
Mosaic CREBBP mutation causes overlapping clinical features of
Rubinstein-Taybi Syndrome: spectrum of CREBBP mutations in Italian
Mosaic CREBBP mutation causes overlapping clinical features of
Characterization of 14 novel deletions underlying Rubinstein–Taybi
Glen MONROE, Postdoc, PhD
Rubinstein–Taybi syndrome in diverse populations - Tekendo
Molecular studies in 10 cases of Rubinstein-Taybi syndrome
Figure 1 from Mutations in CKAP2L, the human homolog of the mouse
Rubinstein-Taybi Syndrome: spectrum of CREBBP mutations in Italian
Lysine Acetylation and Deacetylation in Brain Development and
PDF) Clinical exome sequencing identifies novel CREBBP variants in
Further delineation of an entity caused by CREBBP and EP300
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