Rubinstein-Taybi Syndrome OMIM# 180849 - FDNA™
Por um escritor misterioso
Descrição
A novel CREBBP mutation and its phenotype in a case of Rubinstein
IJMS, Free Full-Text
A submicroscopic deletion involving part of the CREBBP gene
Clinical exome sequencing identifies novel CREBBP variants in 18
PDF) FISH studies in 45 patients with Rubinstein-Taybi syndrome
Rubinstein-Taybi syndrome in a Saudi boy with distinct features
PDF) Evaluation of the immune humoral response of Brazilian
Frontiers Case Report: Low-Level Maternal Mosaicism of a Novel
Rubinstein–Taybi syndrome: clinical and molecular overview
Fetal phenotype of Rubinstein‐Taybi syndrome caused by CREBBP
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