The Rubinstein-Taybi syndrome. Archives of Disease in Childhood
Por um escritor misterioso
Descrição
Forgotten Diseases Research Foundation
Tablet screen medical hi-res stock photography and images - Page 58 - Alamy
PDF] Multiple keloids in a 16-year-old boy with Rubinstein-Taybi syndrome
File:Rubinstein-Taybi Syndrome2.jpg - Wikimedia Commons
Genetic heterogeneity in Rubinstein–Taybi syndrome: delineation of the phenotype of the first patients carrying mutations in EP300
A Case of Rubinstein-Taybi Syndrome with Tetralogy of Fallot
Rubinstein-Taybi syndrome 2 with cerebellar abnormality and neural tube defect. - Abstract - Europe PMC
Born with Rubinstein-Taybi Syndrome (RTS), Braxton and Family are Full of Hope - Global Genes
Exon deletions of the EP300 and CREBBP genes in two children with Rubinstein –Taybi syndrome detected by aCGH
Rubinstein-Taybi Syndrome: spectrum of CREBBP mutations in Italian patients, BMC Medical Genetics
Rubinstein-Taybi Syndrome: Growing Older
Genetic Heterogeneity in Rubinstein-Taybi Syndrome: Mutations in Both the CBP and EP300 Genes Cause Disease - ScienceDirect
Fetal phenotype of Rubinstein‐Taybi syndrome caused by CREBBP mutations - Van‐Gils - 2019 - Clinical Genetics - Wiley Online Library
de
por adulto (o preço varia de acordo com o tamanho do grupo)
