Rubinstein-Taybi syndrome: MedlinePlus Genetics
Por um escritor misterioso
Descrição
Rubinstein-Taybi syndrome is a condition characterized by short stature, moderate to severe intellectual disability, distinctive facial features, and broad thumbs and first toes . Explore symptoms, inheritance, genetics of this condition.
Otopalatodigital Syndrome, Type I disease: Malacards - Research
Fetal phenotype of Rubinstein‐Taybi syndrome caused by CREBBP
Rubinstein-Taybi syndrome: Treatments and life expectancy
Ocular symptoms in patients with Rubinstein-Taybi syndrome; 117
Key Facts
Identification of 22q11.2 deletion in a patient with schizophrenia
Frontiers Behavioral and neuropsychiatric challenges across the
IJMS, Free Full-Text
Exon deletions of the EP300 and CREBBP genes in two children with
Genetic Heterogeneity in Rubinstein-Taybi Syndrome: Mutations in
Novel cAMP binding protein-BP (CREBBP) mutation in a girl with
Rubinstein-Taybi Syndrome: A Complete Overview — DermNet
Rubinstein-Taybi syndrome with scoliosis treated with single-stage
High frequency of copy number imbalances in Rubinstein–Taybi
de
por adulto (o preço varia de acordo com o tamanho do grupo)
