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.
ERG values of 24 patients with Rubinstein-Taybi syndrome
Chromosome 16: MedlinePlus Genetics
:max_bytes(150000):strip_icc()/brittany-ferri-5c42027646e0fb0001964d65.png)
Rubinstein-Taybi Syndrome: Symptoms, Causes, Treatment
PDF] Rubinstein-Taybi syndrome. Review of 732 cases and analysis
Chromosome 16p13.3 Deletion Syndrome, Proximal disease: Malacards
Genetic Heterogeneity in Rubinstein-Taybi Syndrome: Mutations in
IJMS, Free Full-Text
What is RTS? Rubinstein-Taybi Syndrome
PDF) Ocular features in Rubinstein-Taybi syndrome: investigation
Rubinstein-Taybi Syndrome: Genetics
Frontiers Behavioral and neuropsychiatric challenges across the
Identification of de novo EP300 and PLAU variants in a patient
High frequency of copy number imbalances in Rubinstein–Taybi
Frontiers Behavioral and neuropsychiatric challenges across the
Rubinstein-Taybi syndrome: MedlinePlus Genetics
de
por adulto (o preço varia de acordo com o tamanho do grupo)
