Coloboma Associated With Rubinstein-Taybi Syndrome
Descrição
KoreaMed Synapse
Rubinstein–Taybi syndrome - Wikipedia
High frequency of copy number imbalances in Rubinstein–Taybi patients negative to CREBBP mutational analysis
DBMCI MDS : Formerly MDS Experts - RUBINSTEIN TAYBI SYNDROME An autosomal dominant disease associated with deletions of the short arm of ch 16. Clinical Features: - Mental retardation - Broad thumbs
Rubinstein–Taybi syndrome in diverse populations - Tekendo‐Ngongang - 2020 - American Journal of Medical Genetics Part A - Wiley Online Library
Genetics and therapy for pediatric eye diseases - eBioMedicine
Ocular features in Rubinstein-Taybi syndrome: investigation of 24 patients and review of the literature
Genes, Free Full-Text
From Diagnosis to Management : Rubinstein – Taybi Syndrome
Rubinstein-Taybi Syndrome 1
Facial dysmorphism, skeletal anomalies, congenital glucoma, dysplastic nails: Mild Rubinstein-Taybi Syndrome - ScienceDirect
Infantile glaucoma in Rubinstein–Taybi syndrome
Rubinstein-Taybi syndrome (RTS)
de
por adulto (o preço varia de acordo com o tamanho do grupo)
