Rubinstein–Taybi syndrome: clinical and molecular overview, Expert Reviews in Molecular Medicine
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Last updated 20 setembro 2024
Rubinstein–Taybi syndrome: clinical and molecular overview, Expert Reviews in Molecular Medicine
Rubinstein–Taybi syndrome: clinical and molecular overview, Expert Reviews in Molecular Medicine
Rubinstein–Taybi syndrome European Journal of Human Genetics
An unusual presentation of Rubinstein-Taybi Syndrome with bilateral postaxial polydactyly
PDF) Rubinstein-Taybi syndrome: A case report
Rubinstein-Taybi Syndrome: A Case Report
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
Rubinstein–Taybi Syndrome in a Filipino Infant with a Novel CREBBP Gene Pathogenic Variant
Long-term results following osteotomy of the thumb delta phalanx in Rubinstein–Taybi Syndrome - A. Jain, S. Rehman, G. Smith, 2010
PDF) Rubinstein-Taybi Syndrome: A Model of Epigenetic Disorder
PDF) Rubinstein-Taybi syndrome: Clinical features, genetic basis, diagnosis, and management
PDF) Rubinstein-Taybi syndrome: Clinical profile of 11 patients and review of literature
Rubinstein–Taybi syndrome European Journal of Human Genetics
Rubinstein Taybi Syndrome: Most Up-to-Date Encyclopedia, News & Reviews
Frontiers Behavioral and neuropsychiatric challenges across the lifespan in individuals with Rubinstein-Taybi syndrome
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