Rubinstein-Taybi syndrome 2 with cerebellar abnormality and neural
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The association of neural axis and craniovertebral junction
PDF) Electroclinical phenotype in Rubinstein–Taybi syndrome
FIG URE 3 Variability of periventricular posterior white matter
Rubinstein–Taybi syndrome in diverse populations - Tekendo
Congenital Abnormalities of the Brain
Expanding the phenotype associated to KMT2A variants: overlapping
CBP Histone Acetyltransferase Activity Regulates Embryonic Neural
Malformations of Cortical Development
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Genetic dissection of Chiari malformation type 1 using
Rubinstein taybi syndrome
Cerebellar hypoplasia, dysplasia, and enlargement
Genetic heterogeneity in Rubinstein–Taybi syndrome: delineation of
Frontiers An Early Diagnostic Clue for COL18A1- and LAMA1
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