Clinical and mutational spectrum in Korean patients with Rubinstein–Taybi syndrome: The spectrum of brain MRI abnormalities - ScienceDirect
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Two Pathogenic Variants in Two Ultra Rare Syndromes; Smith
PDF) Chemical and genetic rescue of an ep300 knockdown model for
Chemical and genetic rescue of an ep300 knockdown model for
A MT-TL1 variant identified by whole exome sequencing in an
Chemical and genetic rescue of an ep300 knockdown model for
Chemical and genetic rescue of an ep300 knockdown model for
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Fetal phenotype of Rubinstein‐Taybi syndrome caused by CREBBP
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Chromatin remodeling and epigenetic regulation of oligodendrocyte
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