Rubinstein–Taybi syndrome - Wikipedia
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Facial diagnosis of mild and variant CdLS: Insights from a dysmorphologist survey. - Abstract - Europe PMC
Facial dysmorphism, skeletal anomalies, congenital glucoma, dysplastic nails: Mild Rubinstein-Taybi Syndrome - ScienceDirect
Diagnostic analysis of the Rubinstein-Taybi syndrome: five cosmids should be used for microdeletion detection and low number of protein truncating mutations
Pediatric on Squares on X: Rubinstein Taybi Syndrome #Pediatric #Genetics # syndrome / X
Rubinstein-Taybi syndrome: MedlinePlus Genetics
Understanding the role of social media in online health: A global perspective on online social support
Detailed Clinical and Psychological Phenotype of the X-linked HNRNPH2-Related Neurodevelopmental Disorder
Rubinstein–Taybi syndrome in diverse populations - Tekendo‐Ngongang - 2020 - American Journal of Medical Genetics Part A - Wiley Online Library
Rubinstein-Taybi syndrome: clinical features, genetic basis, diagnosis, and management, Italian Journal of Pediatrics
Autism Spectrum Disorder
A case with Rubinstein-Taybi syndrome: A novel frameshift mutation in the CREBBP gene.
Rubinstein-Taybi syndrome: MedlinePlus Genetics
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