Rubinstein-Taybi Syndrome OMIM# 180849 - FDNA™
Descrição
Rubinstein–Taybi syndrome: clinical and molecular overview
Genes, Free Full-Text
PDF) FISH studies in 45 patients with Rubinstein-Taybi syndrome
Identification of de novo EP300 and PLAU variants in a patient
Rubinstein-Taybi syndrome in a Saudi boy with distinct features
A submicroscopic deletion involving part of the CREBBP gene
Rubinstein–Taybi syndrome - Wikipedia
Analysis of mutations within the intron20 splice donor site of
Mosaic CREBBP mutation causes overlapping clinical features of
Rubinstein-Taybi Syndrome 1
Frontiers Case Report: Low-Level Maternal Mosaicism of a Novel
PDF) Exogenous and endogenous HDAC inhibitor effects in Rubinstein
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