Clinical and mutational spectrum in Korean patients with Rubinstein–Taybi syndrome: The spectrum of brain MRI abnormalities - ScienceDirect
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Frontiers Case Report: Low-Level Maternal Mosaicism of a Novel
Epigenetic Mechanisms of Rubinstein–Taybi Syndrome
Translocations Disrupting PHF21A in the Potocki-Shaffer-Syndrome
Chemical and genetic rescue of an ep300 knockdown model for
Epigenetic syndromes with immune deficiency - ScienceDirect
Bi-allelic loss-of-function variants in TMEM147 cause moderate to
7,8-Dihydroxyflavone as a pro-neurotrophic treatment for
PDF) 7,8-Dihydroxyflavone as a pro-neurotrophic treatment for
Chemical and genetic rescue of an ep300 knockdown model for
Epigenetic Mechanisms of Rubinstein–Taybi Syndrome
