Patient Stories Rubinstein-Taybi Syndrome
Por um escritor misterioso
Last updated 31 janeiro 2025
Children who have Rubinstein-Taybi syndrome can, and do, grow and thrive. Find stories of hope from our patients who are living life to the fullest.
Rubinstein-Taybi Syndrome • RTS Support Group
Rubinstein-Taybi Syndrome - an overview
Learning to Speak at Age 18 with a Sister Who Never Quits (Rubinstein-Taybi Syndrome)
Rubinstein-Taybi Syndrome by Alexandra Wilegus
Genetic Heterogeneity in Rubinstein-Taybi Syndrome: Mutations in Both the CBP and EP300 Genes Cause Disease - ScienceDirect
Rubinstein-Taybi Syndrome 1
Exon deletions of the EP300 and CREBBP genes in two children with Rubinstein –Taybi syndrome detected by aCGH
Long-term results following osteotomy of the thumb delta phalanx in Rubinstein–Taybi Syndrome - A. Jain, S. Rehman, G. Smith, 2010
Rubinstein-Taybi syndrome: A report of two siblings with unreported cutaneous stigmata - Indian Journal of Dermatology, Venereology and Leprology
a,b: Patient A at 3 weeks; c,d: Patient B at 6 weeks, note the opening
Patient Stories Rubinstein-Taybi Syndrome
Rubinstein–Taybi syndrome - Wikipedia
Rubinstein-Taybi Syndrome
An approach to a chil with microcephaly
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