Rubinstein-Taybi Syndrome • RTS Support Group
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Rubinstein-Taybi Syndrome (RTS) is an extremely rare genetic condition, occurring in around one person per 125,000 live births.
Rubinstein-Taybi syndrome with scoliosis treated with single-stage posterior spinal fusion: illustrative case in: Journal of Neurosurgery: Case Lessons Volume 1 Issue 11 (2021) Journals
Rubinstein-Taybi syndrome - wikidoc
Rubinstein-Taybi Syndrome: Behavior
Rubinstein-Taybi Syndrome Support Group
Rubinstein-Taybi Syndrome
Epigenetic mechanisms of Rubinstein-Taybi syndrome. - Abstract - Europe PMC
Severe persistent pulmonary hypertension in a neonate with Rubinstein–Taybi syndrome accompanied by triple X syndrome - Pediatrics & Neonatology
Rubinstein–Taybi syndrome: clinical and molecular overview, Expert Reviews in Molecular Medicine
Rubinstein-Taybi syndrome: MedlinePlus Genetics
Understanding the role of social media in online health: A global perspective on online social support
Ocular symptoms in patients with Rubinstein-Taybi syndrome; 117 out of
JCDR - Rubinstein Taybi Syndrome, Oro-facio-dental findings
Rubinstein Taybi Syndrome Awareness RTS Hearts and Ribbon T-Shirt : Clothing, Shoes & Jewelry
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