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rubinstein taybi syndrome
Keloids in Rubinstein–Taybi syndrome: a clinical study - Kar
A novel CREBBP mutation and its phenotype in a case of Rubinstein–Taybi syndrome, BMC Medical Genomics
High frequency of copy number imbalances in Rubinstein–Taybi
Rubinstein Taybi Syndrome Awareness RTS Hearts and
Silas : Rubinstein-Taybi Syndrome » SWEET NECTAR SOCIETY
Broad thumbs and broad hallux: the hallmarks for the Rubinstein
Genetic heterogeneity in Rubinstein–Taybi syndrome: delineation of the phenotype of the first patients carrying mutations in EP300
Dermatologic Manifestations of Rubinstein-Taybi Syndrome Clinical
Genetic heterogeneity in Rubinstein–Taybi syndrome: delineation of
Thyroid Hypoplasia as a Cause of Congenital Hypothyroidism in
The - The Rubinstein-Taybi Syndrome Children's Foundation
A Case of Rubinstein-Taybi Syndrome with Tetralogy of Fallot
Rubinstein-Taybi Syndrome • RTS Support Group
First case report of inherited Rubinstein-Taybi syndrome
Patient Stories Rubinstein-Taybi Syndrome
A case with Rubinstein-Taybi syndrome: A novel frameshift mutation
Loving Leanne: Living with Rubinstein-Taybi Syndrome: Roome
Dentocyclopedia - rubinstein taybi syndrome
Congenital glaucoma as a presenting feature of Rubinstein-Taybi
Rubinstein-Taybi syndrome associated with breast cancer — a case
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