Rubinstein-Taybi syndrome Radiology Reference Article
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Descrição
Rubinstein-Taybi syndrome (RTS) is a very rare genetic multi-system disorder primarily characterised by intellectual disability, broad and often angulated thumbs and halluces, and distinctive facia
This photograph is a panoramic radiograph of the dentition prior
Expanding the phenotypic spectrum in EP300‐related Rubinstein
Low bone mineral density on DXA and slipped capital femoral
Low bone mineral density on DXA and slipped capital femoral
Clinical and mutational spectrum in Korean patients with
Incidence and Spectrum of Renal Complications and Extrarenal
IJMS, Free Full-Text
a) Showing broad thumbs, (b) X-ray of hands of another patient
Ocular features in Rubinstein-Taybi syndrome: investigation of 24
Clinodactyly, Radiology Reference Article
Figure 1 from Rubinstein-Taybi Syndrome in a 19-years old boy
Surgical treatment of scoliosis in Rubinstein-Taybi syndrome type
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