Ultra-Rare Syndromes: The Example of Rubinstein-Taybi Syndrome
Por um escritor misterioso
Descrição
CBP-HSF2 structural and functional interplay in Rubinstein-Taybi neurodevelopmental disorder
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: A Rare Case Report
Diagnostically relevant facial gestalt information from ordinary photos
Rubinstein-Taybi Syndrome: A Complete Overview — DermNet
Forgotten Diseases Research Foundation
Rubinstein–Taybi Syndrome in a Filipino Infant with a Novel CREBBP Gene Pathogenic Variant
Dermatologic Manifestations of Rubinstein-Taybi Syndrome Clinical Presentation: History, Physical Examination, Complications
PDF] Rubinstein-Taybi Syndrome: A Case Report
Dermatologic Manifestations of Rubinstein-Taybi Syndrome: Background, Pathophysiology, Etiology
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