Rubinstein-Taybi syndrome - wikidoc
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Last updated 21 setembro 2024
Rubinstein-Taybi syndrome: MedlinePlus Genetics
Radiology Quiz 22377
Molecular studies in 10 cases of Rubinstein-Taybi syndrome, including a mild variant showing a missense mutation in codon 1175 of CREBBP
Rubinstein–Taybi syndrome European Journal of Human Genetics
Rubinstein-Taybi syndrome: MedlinePlus Genetics
Rubinstein–Taybi syndrome - Wikipedia
Rubinstein-Taybi syndrome
Rubinstein-Taybi syndrome - Atlas of Human Malformation Syndromes in Diverse Populations
Rubinstein-Taybi syndrome: MedlinePlus Genetics
Genetic heterogeneity in Rubinstein–Taybi syndrome: delineation of the phenotype of the first patients carrying mutations in EP300
Pediatric on Squares on X: Rubinstein Taybi Syndrome #Pediatric #Genetics # syndrome / X
DBMCI MDS : Formerly MDS Experts - RUBINSTEIN TAYBI SYNDROME An autosomal dominant disease associated with deletions of the short arm of ch 16. Clinical Features: - Mental retardation - Broad thumbs
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