RUBINSTEIN TAYBI SYNDROME An autosomal dominant disease associated
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Congenital glaucoma as a presenting feature of Rubinstein-Taybi syndrome in an infant with a novel pathogenic variant in the CREBBP gene
Rubinstein‐Taybi syndrome in Chinese population with four novel mutations - Yu - 2021 - American Journal of Medical Genetics Part A - Wiley Online Library
Rubinstein-Taybi Syndrome
A Case of Rubinstein-Taybi Syndrome with Tetralogy of Fallot
IJMS, Free Full-Text
Rubinstein-Taybi syndrome in a Saudi boy with distinct features and variants in both the CREBBP and EP300 genes: a case report, BMC Medical Genetics
Ocular features in Rubinstein-Taybi syndrome: investigation of 24 patients and review of the literature
Rubinstein-Taybi Syndrome - an overview
Rubinstein–Taybi syndrome - Wikipedia
Rubinstein-Taybi Syndrome: A case report
Molecular studies in 10 cases of Rubinstein-Taybi syndrome, including a mild variant showing a missense mutation in codon 1175 of CREBBP
Rubinstein-Taybi syndrome: MedlinePlus Genetics
Rubenstein-Taybi syndrome, Psychology Wiki
Rubinstein-Taybi Syndrome Awareness
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