Riley H., Smith W.Macrocephaly, pseudopapilledema and multiple hemangiomata: a previously undescribed heredofamilial syndrome. Pediatrics. 1960;26:293-300.
4.
Bannayan G.Lipomatosis, angiomatosis and macrocephaly. Arch Pathol. 1971;92:1-5.
5.
Ruvalcaba R., Myhre S., Smith D.Sotos syndrome with intestinal polyps, and pigmentary changes of the genitalia . Clin Genet. 1980;18:413-416.
6.
Cohen M.Bannayan-Riley-Ruvalcaba syndrome: renaming three formerly recognized syndromes as one etiologic entity. Am J Med Genet. 1990 ;35:291.
7.
Zigman A., Lavine J., Jones M., Boland R., Carethers J.Localization of the Bannayan-Riley-Ruvalcaba syndrome gene to chromosome 10Q23 . Gastroenterology. 1997;113:1433-1437.
8.
Arch E., Goodman B., VanWesep R., et al. Deletion of PTEN in a patient with Bannayan-Riley-Ruvalcaba syndrome suggests allelism with Cowden disease. Am J Med Genet . 1997;71:489-493.
9.
Marsh D., Kum J., Lunetta K., et al. PTEN mutation spectrum and genotype-phenotype correlations in Bannayan-Riley-Ruvalcaba syndrome suggests a single entity with Cowden syndrome . Hum Mol Genet. 1999; 8:1461-1472.
10.
Mahmood MN, Salama ME, Chaffins M., et al. Solitary sclerotic fibroma of skin: a possible link with pleomorphic fibroma with immunophenotypic expression for 013 (CD99) and CD34. J Cutan Pathol. 2003;10:631-636.
11.
Kamino H., Lee JY, Berke A.Pleomorphic fibroma of the skin: a benign neoplasm with cytologic atypia: a clincopathologic study of eight cases. Am J Surg Pathol . 1989;13:107-113.
12.
Kato N., Kimura K., Suguwara H., Aoyagi S., Ikeda T., Horii A.Germline mutation of the PTEN gene in a Japanese patient with Cowden disease . Int J Oncol. 2001;18: 1017-1022.
13.
Hendricks Y. , Verhallen J., van der Smagt J., et al. Bannayan-Riley-Ruvalcaba syndrome: further delineation of the phenotype and management of PTEN mutation-positive cases. Fam Cancer. 2003;2:79-85.