4 Newborn with Rubinstein-Taybi syndrome showing microcephaly
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Ultrasound 2-D and 3-D diagnosis of Rubinstein–Taybi syndrome in a 21-week-old fetus
A Case of Rubinstein-Taybi Syndrome with Tetralogy of Fallot
Rubinstein-Taybi Syndrome: A Complete Overview — DermNet
Genetic heterogeneity in Rubinstein–Taybi syndrome: delineation of the phenotype of the first patients carrying mutations in EP300
Rubinstein–Taybi syndrome in diverse populations - Tekendo‐Ngongang - 2020 - American Journal of Medical Genetics Part A - Wiley Online Library
Genetic heterogeneity in Rubinstein–Taybi syndrome: delineation of the phenotype of the first patients carrying mutations in EP300
Rubinstein-Taybi 2 associated to novel EP300 mutations: deepening the clinical and genetic spectrum, BMC Medical Genetics
Forgotten Diseases Research Foundation
A case with Rubinstein-Taybi syndrome: A novel frameshift mutation in the CREBBP gene.
Microcephaly: Symptoms, Causes & Outlook
4 Newborn with Rubinstein-Taybi syndrome showing microcephaly, frontal
4 Newborn with Rubinstein-Taybi syndrome showing microcephaly, frontal
An approach to a chil with microcephaly
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