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.
Rubinstein-Taybi syndrome - wikidoc
Fetal phenotype of Rubinstein‐Taybi syndrome caused by CREBBP
Chromosome 16p13.3 Deletion Syndrome, Proximal disease: Malacards
Frontiers Behavioral and neuropsychiatric challenges across the
Chromosome 16: MedlinePlus Genetics
Role of the ADCY9 gene in cardiac abnormalities of the Rubinstein
Rubinstein-Taybi syndrome: MedlinePlus Genetics
Frontiers Genetic Diagnosis of Rubinstein–Taybi Syndrome With
Rubinstein-Taybi Syndrome: Genetics
Frontiers Behavioral and neuropsychiatric challenges across the
Empirical Literature on Rubinstein-Taybi Syndrome (RTS) Meeting
Molecular studies in 10 cases of Rubinstein-Taybi syndrome
PDF) Ocular features in Rubinstein-Taybi syndrome: investigation
Novel cAMP binding protein-BP (CREBBP) mutation in a girl with
de
por adulto (o preço varia de acordo com o tamanho do grupo)
