Rubinstein–Taybi syndrome: clinical and molecular overview, Expert Reviews in Molecular Medicine
Por um escritor misterioso
Last updated 19 maio 2024
Frontiers Genetic Diagnosis of Rubinstein–Taybi Syndrome With Multiplex Ligation-Dependent Probe Amplification (MLPA) and Whole-Exome Sequencing (WES): Case Series With a Novel CREBBP Variant
Psychiatric Profile in Rubinstein-Taybi Syndrome
Genes, Free Full-Text
PDF) A novel EP300 mutation associated with Rubinstein-Taybi syndrome type 2 presenting as combined immunodeficiency
Rubinstein–Taybi syndrome European Journal of Human Genetics
An unusual presentation of Rubinstein-Taybi Syndrome with bilateral postaxial polydactyly
PDF) Rubinstein-Taybi Syndrome: A Model of Epigenetic Disorder
IJMS, Free Full-Text
Rubinstein-Taybi Syndrome 2 disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials
Frontiers Behavioral and neuropsychiatric challenges across the lifespan in individuals with Rubinstein-Taybi syndrome
Rubinstein Taybi Syndrome: Most Up-to-Date Encyclopedia, News & Reviews
Epigenetic Mechanisms of Rubinstein–Taybi Syndrome
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