Facial features of Rubinstein-Taybi syndrome
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Rubinstein–Taybi syndrome - Wikipedia
Rubinstein-Taybi Syndrome: A Complete Overview — DermNet
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
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Rubinstein-Taybi Syndrome: Symptoms, Causes, Treatment
Facial dysmorphism, skeletal anomalies, congenital glucoma, dysplastic nails: Mild Rubinstein-Taybi Syndrome - ScienceDirect
Identification of de novo EP300 and PLAU variants in a patient with Rubinstein–Taybi syndrome-related arterial vasculopathy and skeletal anomaly
Genetic heterogeneity in Rubinstein–Taybi syndrome: delineation of the phenotype of the first patients carrying mutations in EP300
Rubinstein-Taybi Syndrome: A Pediatric Case Report
Rubinstein Taybi Syndrome in an Indian Child due to EP300 Gene Mutation
Born with Rubinstein-Taybi Syndrome (RTS), Braxton and Family are Full of Hope - Global Genes
Rubinstein Taybi Syndrome - MEDizzy
Ocular features in Rubinstein-Taybi syndrome: investigation of 24 patients and review of the literature
First case report of inherited Rubinstein-Taybi syndrome associated with a novel EP300 variant, BMC Medical Genetics
Genetic heterogeneity in Rubinstein–Taybi syndrome: delineation of the phenotype of the first patients carrying mutations in EP300
Two adults with Rubinstein–Taybi syndrome with mild mental retardation, glaucoma, normal growth and skull circumference, and camptodactyly of third fingers - Wieczorek - 2009 - American Journal of Medical Genetics Part A
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