Rubinstein–Taybi syndrome: clinical and molecular overview, Expert Reviews in Molecular Medicine
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Oral and Dental Manifestations in Rubinstein-Taybi Syndrome: Report of a Rare Case
Molecular studies in 10 cases of Rubinstein-Taybi syndrome, including a mild variant showing a missense mutation in codon 1175 of CREBBP
Frontiers Behavioral and neuropsychiatric challenges across the lifespan in individuals with Rubinstein-Taybi syndrome
PDF] Rubinstein-Taybi Syndrome: A Female Patient with a De Novo Reciprocal Translocation T(2; 16)(Q36.3; P13.3) and Dysgranulopoiesis
Rubinstein-Taybi Syndrome: A Case Report
First case report of inherited Rubinstein-Taybi syndrome associated with a novel EP300 variant, BMC Medical Genetics
PDF) Rubinstein-Taybi syndrome: Clinical features, genetic basis, diagnosis, and management
Frontiers Behavioral and neuropsychiatric challenges across the lifespan in individuals with Rubinstein-Taybi syndrome
PDF) Rubinstein-Taybi syndrome: Dental manifestations and management
Epigenetic mechanisms of Rubinstein-Taybi syndrome. - Abstract - Europe PMC
PDF] Rubinstein-Taybi Syndrome Associated with Pituitary Macroadenoma: A Case Report
Rubinstein-Taybi Syndrome: A Case Report
PDF] Rubinstein-Taybi Syndrome in a 19-years old boy.
Ocular features in Rubinstein-Taybi syndrome: investigation of 24 patients and review of the literature
Analysis of mutations within the intron20 splice donor site of CREBBP in patients with and without classical RSTS
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