Rubinstein–Taybi syndrome: clinical and molecular overview, Expert Reviews in Molecular Medicine
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Cureus, Rubinstein-Taybi Syndrome Associated with Pituitary Macroadenoma: A Case Report
Congenital glaucoma as a presenting feature of Rubinstein-Taybi syndrome in an infant with a novel pathogenic variant in the CREBBP gene
Genes, Free Full-Text
PDF) Rubinstein-Taybi Syndrome: A Case Report
IJMS, Free Full-Text
Genes, Free Full-Text
CBP-HSF2 structural and functional interplay in Rubinstein-Taybi neurodevelopmental disorder
Frontiers Behavioral and neuropsychiatric challenges across the lifespan in individuals with Rubinstein-Taybi syndrome
PDF] Rubinstein-Taybi Syndrome in a 19-years old boy.
Exon deletions of the EP300 and CREBBP genes in two children with Rubinstein –Taybi syndrome detected by aCGH
Oral and Dental Manifestations in Rubinstein-Taybi Syndrome: Report of a Rare Case
Genes, Free Full-Text
Clinical and Experimental Pediatrics
Opposing Effects of CREBBP Mutations Govern the Phenotype of Rubinstein-Taybi Syndrome and Adult SHH Medulloblastoma - ScienceDirect
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