These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
6. Cowden's syndrome report of a case with malignant melanoma. Siegel JM; Reed WB Pahlavi Med J; 1976 Apr; 7(2):262-9. PubMed ID: 1272600 [No Abstract] [Full Text] [Related]
7. EEC syndrome: report on 20 new patients, clinical and genetic considerations. Rodini ES; Richieri-Costa A Am J Med Genet; 1990 Sep; 37(1):42-53. PubMed ID: 2240042 [TBL] [Abstract][Full Text] [Related]
8. [Cowden's disease]. Nudenberg B; Pöex A; Escovich L; Reeves G; Alonso H; Sarano H Med Cutan Ibero Lat Am; 1977; 5(1):47-51. PubMed ID: 561275 [TBL] [Abstract][Full Text] [Related]
10. Cowden's syndrome affecting the mouth, gastrointestinal, and central nervous system: a case report and review of the literature. Leão JC; Batista V; Guimarães PB; Belo J; Porter SR Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 2005 May; 99(5):569-72. PubMed ID: 15829879 [TBL] [Abstract][Full Text] [Related]
11. Multiple hamartoma syndrome (Cowden's syndrome): case report and literature review. Wright DD; Whitney J Gen Dent; 2006; 54(6):417-9. PubMed ID: 17134080 [TBL] [Abstract][Full Text] [Related]
12. Setleis (bitemporal 'forceps marks') syndrome in a German family: evidence for autosomal dominant inheritance. Artlich A; Schwinger E; Meinecke P Clin Dysmorphol; 1992 Jul; 1(3):157-60. PubMed ID: 1342863 [TBL] [Abstract][Full Text] [Related]