RUBINSTEIN TAYBI SYNDROME An autosomal dominant disease associated
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Rubinstein-Taybi syndrome: Multisystem involvement and its clinical
Rubinstein-Taybi syndrome: MedlinePlus Genetics
Rubinstein–Taybi syndrome - Wikipedia
Rubinstein-Taybi syndrome 2 with cerebellar abnormality and neural tube defect. - Abstract - Europe PMC
Mosaic CREBBP mutation causes overlapping clinical features of Rubinstein– Taybi and Filippi syndromes
Fetal phenotype of Rubinstein‐Taybi syndrome caused by CREBBP mutations - Van‐Gils - 2019 - Clinical Genetics - Wiley Online Library
CBP-HSF2 structural and functional interplay in Rubinstein-Taybi neurodevelopmental disorder
Divergent variant patterns among 19 patients with Rubinstein‐Taybi syndrome uncovered by comprehensive genetic analysis including whole genome sequencing - Enomoto - 2022 - Clinical Genetics - Wiley Online Library
Rubinstein-Taybi Syndrome
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JCDR - Rubinstein-Taybi syndrome, Clinodactyly, Talon cusps
Rubinstein-Taybi Syndrome
Ultrasound 2-D and 3-D diagnosis of Rubinstein–Taybi syndrome in a 21-week-old fetus
Multiple pilomatricomas in twins with Rubinstein-Taybi syndrome
Genetic heterogeneity in Rubinstein–Taybi syndrome: delineation of the phenotype of the first patients carrying mutations in EP300
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