The - The Rubinstein-Taybi Syndrome Children's Foundation
Por um escritor misterioso
Last updated 21 fevereiro 2025
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Rubenstein Taybi Syndrome Oral and Dental Features Carol Mason Consultant in Paediatric Dentistry Great Ormond Street Hospital for Children NHS Foundation. - ppt download
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PDF) Rubinstein-Taybi syndrome medical guidelines
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Clinical photos of the patients. (a) Case 1: Dysmorphic facial features
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Genes, Free Full-Text
Our - The Rubinstein-Taybi Syndrome Children's Foundation
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Patient Stories Rubinstein-Taybi Syndrome
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Rubinstein Taybi Syndrome in an Indian Child due to EP300 Gene Mutation
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Rubinstein-Taybi Syndrome • RTS Support Group
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Logo for Rare Disease Research Foundation by Rtscf
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First case of Rubinstein–Taybi syndrome with desquamation associated with a novel mutation in the bromodomain of the CREBBP gene - Wang - 2019 - Clinical and Experimental Dermatology - Wiley Online Library
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Special Friends Foundation
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Molecular studies in 10 cases of Rubinstein-Taybi syndrome, including a mild variant showing a missense mutation in codon 1175 of CREBBP
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Rubinstein-Taybi syndrome 2 with cerebellar abnormality and neural tube defect. - Abstract - Europe PMC
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