Cowden Syndrome
Author:
Publisher
Springer International Publishing
Link
https://link.springer.com/content/pdf/10.1007/978-3-030-62345-6_5217
Reference20 articles.
1. Browning, M. J., Chandra, A., Carbonaro, V., Okkenhaug, K., & Barwell, J. (2015). Cowden’s syndrome with immunodeficiency. Journal of Medical Genetics, 52(12), 856–859.
2. Bubien, V., Bonnet, F., Brouste, V., Hoppe, S., Barouk-Simonet, E., David, A., et al. (2013). French Cowden Disease Network. High cumulative risks of cancer in patients with PTEN hamartoma tumour syndrome. Journal of Medical Genetics, 50(4), 255–263.
3. Cameselle-Teijeiro, J., Fachal, C., Cabezas-Agrícola, J., Alfonsín-Barreiro, N., AbdulkaderNallib, I., Vega, A., & Hermo, J. (2015). Thyroid pathology findings in Cowden syndrome: A clue for the diagnosis of the PTEN hamartoma tumor syndrome. American Journal of Clinical Pathology, 144, 322–328.
4. Cavaillé, M., Ponelle-Chachuat, F., Uhrhammer, N., Viala, S., Gay-Bellile, M., Privat, M., et al. (2018). Early onset multiple primary tumors in atypical presentation of Cowden syndrome identified by whole-exome-sequencing. Frontiers in Genetics, 9, 353.
5. Eng, C. (2000). Will the real Cowden syndrome please stand up: Revised diagnostic criteria. Journal of Medical Genetics, 37(11), 828–830.
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