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Fetal phenotype of Rubinstein‐Taybi syndrome caused by CREBBP

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Fetal phenotype of Rubinstein‐Taybi syndrome caused by CREBBP
CBP Histone Acetyltransferase Activity Regulates Embryonic Neural Differentiation in the Normal and Rubinstein-Taybi Syndrome Brain: Developmental Cell
Fetal phenotype of Rubinstein‐Taybi syndrome caused by CREBBP
Genes, Free Full-Text
Fetal phenotype of Rubinstein‐Taybi syndrome caused by CREBBP
Rubinstein-Taybi Syndrome
Fetal phenotype of Rubinstein‐Taybi syndrome caused by CREBBP
CBP Histone Acetyltransferase Activity Regulates Embryonic Neural Differentiation in the Normal and Rubinstein-Taybi Syndrome Brain: Developmental Cell
Fetal phenotype of Rubinstein‐Taybi syndrome caused by CREBBP
Opposing Effects of CREBBP Mutations Govern the Phenotype of Rubinstein-Taybi Syndrome and Adult SHH Medulloblastoma - ScienceDirect
Fetal phenotype of Rubinstein‐Taybi syndrome caused by CREBBP
Rubinstein Taybi Syndrome: Most Up-to-Date Encyclopedia, News & Reviews
Fetal phenotype of Rubinstein‐Taybi syndrome caused by CREBBP
Rubinstein-Taybi Syndrome
Fetal phenotype of Rubinstein‐Taybi syndrome caused by CREBBP
Surgical treatment of scoliosis in Rubinstein-Taybi syndrome type 2: a case report – topic of research paper in Clinical medicine. Download scholarly article PDF and read for free on CyberLeninka open science
Fetal phenotype of Rubinstein‐Taybi syndrome caused by CREBBP
Rubinstein-Taybi syndrome: MedlinePlus Genetics
Fetal phenotype of Rubinstein‐Taybi syndrome caused by CREBBP
Characterization of 14 novel deletions underlying Rubinstein–Taybi syndrome: an update of the CREBBP deletion repertoire
Fetal phenotype of Rubinstein‐Taybi syndrome caused by CREBBP
Opposing Effects of CREBBP Mutations Govern the Phenotype of Rubinstein-Taybi Syndrome and Adult SHH Medulloblastoma - ScienceDirect
Fetal phenotype of Rubinstein‐Taybi syndrome caused by CREBBP
Rubinstein-Taybi syndrome (RTS)
Fetal phenotype of Rubinstein‐Taybi syndrome caused by CREBBP
Fetal phenotype of Rubinstein‐Taybi syndrome caused by CREBBP mutations - Van‐Gils - 2019 - Clinical Genetics - Wiley Online Library
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