Fetal phenotype of Rubinstein‐Taybi syndrome caused by CREBBP
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CBP-HSF2 structural and functional interplay in Rubinstein-Taybi neurodevelopmental disorder
PDF) Rubinstein-Taybi syndrome medical guidelines
CBP Histone Acetyltransferase Activity Regulates Embryonic Neural Differentiation in the Normal and Rubinstein-Taybi Syndrome Brain: Developmental Cell
IJMS, Free Full-Text
IJMS, Free Full-Text
PDF) Rubinstein-Taybi syndrome medical guidelines
Opposing Effects of CREBBP Mutations Govern the Phenotype of Rubinstein-Taybi Syndrome and Adult SHH Medulloblastoma - ScienceDirect
IJMS, Free Full-Text
IJMS, Free Full-Text
Rubinstein–Taybi syndrome: clinical and molecular overview, Expert Reviews in Molecular Medicine
Rubinstein-Taybi syndrome 2 with cerebellar abnormality and neural tube defect. - Abstract - Europe PMC
Rubinstein–Taybi syndrome: clinical and molecular overview, Expert Reviews in Molecular Medicine
A case with Rubinstein-Taybi syndrome: A novel frameshift mutation in the CREBBP gene.
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