Rubinstein-Taybi Syndrome OMIM# 180849 - FDNA™
Por um escritor misterioso
Descrição
CBP-HSF2 structural and functional interplay in Rubinstein-Taybi
IJMS, Free Full-Text
High frequency of copy number imbalances in Rubinstein–Taybi
A novel CREBBP mutation and its phenotype in a case of Rubinstein
CBP/EP300 acetylates and stabilizes the stress-responsive Heat
Insights into genotype–phenotype correlations from CREBBP point
Frontiers Case Report: Low-Level Maternal Mosaicism of a Novel
PDF) Clinical exome sequencing identifies novel CREBBP variants in
Clinical exome sequencing identifies novel CREBBP variants in 18
Rubinstein-Taybi syndrome in a Saudi boy with distinct features
Frontiers Case Report: Low-Level Maternal Mosaicism of a Novel
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