Rubinstein-Taybi syndrome 2 with cerebellar abnormality and neural
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Last updated 21 setembro 2024
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Identification of de novo EP300 and PLAU variants in a patient
Rubinstein-Taybi syndrome: clinical features, genetic basis
Rubinstein-Taybi syndrome: MedlinePlus Genetics
Congenital basis of posterior fossa anomalies - Claudia Cotes
Molecular studies in 10 cases of Rubinstein-Taybi syndrome
Opposing Effects of CREBBP Mutations Govern the Phenotype of
Malformations of Cortical Development
Facial dysmorphism, skeletal anomalies, congenital glucoma
Life, Free Full-Text
Clinical and mutational spectrum in Korean patients with
Rubinstein-Taybi Syndrome
Genetic dissection of Chiari malformation type 1 using
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