Rubinstein-Taybi syndrome - Atlas of Human Malformation Syndromes in Diverse Populations
Por um escritor misterioso
Last updated 16 junho 2024
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Rubinstein-Taybi Syndrome: A case report
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Congenital Malformations and Syndromes: Early Diagnosis and
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The Syndromal Child
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Mosaic CREBBP mutation causes overlapping clinical features of
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Facial dysmorphism, skeletal anomalies, congenital glucoma
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Rubinstein-Taybi syndrome: clinical features, genetic basis
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Slow development causes, understanding global developmental delay
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Facial dysmorphism, skeletal anomalies, congenital glucoma
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Rubinstein–Taybi syndrome - Wikipedia
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NRF1 Association with AUTS2-Polycomb Mediates Specific Gene
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NIH Creates Atlas of Human Malformation Syndromes in Diverse
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Orodental abnormalities in limb malformation syndromes: A review
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Coffin-Lowry Syndrome disease: Malacards - Research Articles
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Glaucoma and Findings Simulating Glaucoma in the Rubinstein-Taybi
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