Pediatric on Squares on X: Rubinstein Taybi Syndrome #Pediatric
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A novel CREBBP mutation and its phenotype in a case of Rubinstein–Taybi syndrome, BMC Medical Genomics
Molecular studies in 10 cases of Rubinstein-Taybi syndrome, including a mild variant showing a missense mutation in codon 1175 of CREBBP
Mosaic CREBBP mutation causes overlapping clinical features of Rubinstein– Taybi and Filippi syndromes
Figure 1 from Rubinstein-Taybi Syndrome in a 19-years old boy.
Rubinstein-Taybi Syndrome: Growing Older
Rubinstein-Taybi Syndrome: Orthopaedics
Dutch child (6) with Rubinstein-Taybi Syndrome (RTS) during speech therapy
Rubinstein-Taybi Syndrome: Genetics
Rubinstein-Taybi syndrome: MedlinePlus Genetics
Rubinstein-Taybi syndrome: Multisystem involvement and its clinical
Rubinstein–Taybi syndrome in diverse populations - Tekendo‐Ngongang - 2020 - American Journal of Medical Genetics Part A - Wiley Online Library
A case with Rubinstein-Taybi syndrome: A novel frameshift mutation in the CREBBP gene.
Rubinstein-Taybi Syndrome: Growing Older
Rubinstein‐Taybi syndrome medical guidelines - Wiley - 2003 - American Journal of Medical Genetics Part A - Wiley Online Library
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