Tumor Screening in Beckwith-Wiedemann Syndrome: Parental Perspectives
Author:
Funder
National Cancer Institute
Alex's Lemonade Stand Foundation for Childhood Cancer (US)
St. Baldrick's Foundation (US)
Publisher
Wiley
Subject
Genetics (clinical)
Link
http://link.springer.com/article/10.1007/s10897-017-0182-8/fulltext.html
Reference35 articles.
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2. Brioude, F., Lacoste, A., Netchine, I., Vazquez, M. P., Auber, F., Audry, G., et al. (2013). Beckwith-Wiedemann syndrome: Growth pattern and tumor risk according to molecular mechanism, and guidelines for tumor surveillance. Hormone Research in Pædiatrics, 80(6), 457–465. https://doi.org/10.1159/000355544 .
3. Budych, K., Helms, T. M., & Schultz, C. (2012). How do patients with rare diseases experience the medical encounter? Exploring role behavior and its impact on patient-physician interaction. Health Policy, 105(2–3), 154–164. https://doi.org/10.1016/j.healthpol.2012.02.018 .
4. Choyke, P. L., Siegel, M. J., Craft, A. W., Green, D. M., & DeBaun, M. R. (1999). Screening for Wilms tumor in children with Beckwith-Wiedemann syndrome or idiopathic hemihypertrophy. Medical and Pediatric Oncology, 32(3), 196–200.
5. Clericuzio, C. L., & Martin, R. A. (2009). Diagnostic criteria and tumor screening for individuals with isolated hemihyperplasia. Genetics in Medicine, 11(3), 220–222. https://doi.org/10.1097/GIM.0b013e31819436cf .
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