RUBINSTEIN TAYBI SYNDROME An autosomal dominant disease associated
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Forgotten Diseases Research Foundation
Rubinstein-Taybi Syndrome: A Complete Overview — DermNet
What Is Rubinstein-Taybi Syndrome? - StoryMD
Rubinstein-Taybi Syndrome: spectrum of CREBBP mutations in Italian patients, BMC Medical Genetics
Rubinstein–Taybi syndrome in diverse populations - Tekendo‐Ngongang - 2020 - American Journal of Medical Genetics Part A - Wiley Online Library
Rubinstein-Taybi Syndrome: A case report
Rubinstein-Taybi Syndrome
PDF) Broad thumbs and broad hallux: The hallmarks for the Rubinstein-Taybi syndrome
PDF) Epigenetic Mechanisms of Rubinstein–Taybi Syndrome
Congenital glaucoma as a presenting feature of Rubinstein-Taybi syndrome in an infant with a novel pathogenic variant in the CREBBP gene
Genetic heterogeneity in Rubinstein–Taybi syndrome: delineation of the phenotype of the first patients carrying mutations in EP300
Egyptian sibs with autosomal recessive Robinow syndrome. Note
A Case of Rubinstein-Taybi Syndrome with Tetralogy of Fallot
PDF] Dental treatment of a child with Rubinstein-Taybi syndrome.
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