Rubinstein-Taybi Syndrome
Por um escritor misterioso
Last updated 22 fevereiro 2025
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The Rubinstein-Taybi Syndrome Program provides expert confirmation of diagnosis as well as the latest treatments and support. Explore our offerings.
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The Ridenour Family - RareKC
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Rubinstein–Taybi syndrome - Wikipedia
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Rubinstein-Taybi syndrome-showing distinctive clinical features
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Fetal phenotype of Rubinstein‐Taybi syndrome caused by CREBBP
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Genetic heterogeneity in Rubinstein–Taybi syndrome: delineation of
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Learning to Speak at Age 18 with a Sister Who Never Quits
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Rubinstein Taybi Syndrome in an Indian Child due to EP300 Gene
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Facial dysmorphism, skeletal anomalies, congenital glucoma
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Genetic heterogeneity in Rubinstein–Taybi syndrome: delineation of
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A Case of Rubinstein-Taybi Syndrome with Tetralogy of Fallot
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Forgotten Diseases Research Foundation
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Patient Stories Rubinstein-Taybi Syndrome
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Forgotten Diseases Research Foundation
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Rubinstein Syndrome - an overview
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Rubinstein-Taybi Syndrome
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