Rubinstein‐Taybi syndrome in Chinese population with four novel
Por um escritor misterioso
Descrição
Frontiers Case report: A preterm infant with rubinstein-taybi
Ocular symptoms in patients with Rubinstein-Taybi syndrome; 117
Rubinstein–Taybi syndrome: clinical and molecular overview
A novel CREBBP mutation and its phenotype in a case of Rubinstein
PDF) Clinical exome sequencing identifies novel CREBBP variants in
Exon deletions of the EP300 and CREBBP genes in two children with
Children, Free Full-Text
Rubinstein–Taybi syndrome: clinical and molecular overview
Ocular symptoms in patients with Rubinstein-Taybi syndrome; 117
Rubinstein-Taybi Syndrome (RTS) Research
A Novel CREBBP in-Frame Deletion Variant in a Chinese Girl with
Clinical exome sequencing identifies novel CREBBP variants in 18
PDF) Rubinstein-Taybi Syndrome: A Model of Epigenetic Disorder
Frontiers Case report: A preterm infant with rubinstein-taybi
A novel CREBBP mutation and its phenotype in a case of Rubinstein
de
por adulto (o preço varia de acordo com o tamanho do grupo)
