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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