Rubinstein–Taybi syndrome European Journal of Human Genetics
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Last updated 17 junho 2024
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Genes, Free Full-Text
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Rubinstein-Taybi Syndrome: spectrum of CREBBP mutations in Italian patients, BMC Medical Genetics
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A Case of Rubinstein-Taybi Syndrome with Tetralogy of Fallot
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Epigenetic Mechanisms of Rubinstein–Taybi Syndrome
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A case of bilateral elbow dislocation in a patient with Rubinstein-Taybi syndrome - JSES International
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Rubinstein Taybi Syndrome: Most Up-to-Date Encyclopedia, News & Reviews
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Rubinstein‐Taybi syndrome in Chinese population with four novel mutations - Yu - 2021 - American Journal of Medical Genetics Part A - Wiley Online Library
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Expanding the phenotype associated to KMT2A variants: overlapping clinical signs between Wiedemann–Steiner and Rubinstein–Taybi syndromes
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Mosaic CREBBP mutation causes overlapping clinical features of Rubinstein– Taybi and Filippi syndromes
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Rubinstein–Taybi syndrome in diverse populations - Tekendo‐Ngongang - 2020 - American Journal of Medical Genetics Part A - Wiley Online Library
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IJMS, Free Full-Text
Volume 19 Issue 1, January 2011
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Frontiers Case Report: Low-Level Maternal Mosaicism of a Novel CREBBP Variant Causes Recurrent Rubinstein-Taybi Syndrome in Two Siblings of a Chinese Family
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