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rubinstein taybi genereviews
Cockayne Syndrome: Most Up-to-Date Encyclopedia, News & Reviews
(PDF) Identification of de novo EP300 and PLAU variants in a patient with Rubinstein–Taybi syndrome-related arterial vasculopathy and skeletal anomaly
Identification of de novo EP300 and PLAU variants in a patient with Rubinstein–Taybi syndrome-related arterial vasculopathy and skeletal anomaly
Forgotten Diseases Research Foundation
Rubinstein-Taybi Syndrome 2 disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials
What is CdLS? Ben and his Brothers: Life with 4 boys and CdLS
Expanding the phenotype associated to KMT2A variants: overlapping clinical signs between Wiedemann–Steiner and Rubinstein–Taybi syndromes
NRF1 Association with AUTS2-Polycomb Mediates Specific Gene Activation in the Brain
Rubinstein–Taybi syndrome in diverse populations - Tekendo
Rubinstein-Taybi syndrome: principal oral and dental disorders and literature update
Rubinstein–Taybi syndrome - Wikipedia
PDF) The behavioral phenotype of Rubinstein–Taybi syndrome: A scoping review of the literature
Genes, Free Full-Text
genereviews.org - GeneReviews® - NCBI Bookshelf
Rubinstein-Taybi syndrome: principal oral and dental disorders and
Rubinstein-Taybi Syndrome - GeneReviews® - NCBI Bookshelf
Approach to inherited hypertrichosis: A brief review - Indian
Rubinstein Taybi syndrome causes, symptoms, diagnosis, treatment & prognosis
Silver Russell Syndrome: Most Up-to-Date Encyclopedia, News & Reviews
A novel CREBBP mutation and its phenotype in a case of Rubinstein
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