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3. Ruvalcaba-Myhre-Smith syndrome: a case with probable autosomal-dominant inheritance and additional manifestations. DiLiberti JH; Weleber RG; Budden S Am J Med Genet; 1983 Jul; 15(3):491-5. PubMed ID: 6881215 [TBL] [Abstract][Full Text] [Related]
4. Cerebral gigantism, intestinal polyposis, and pigmentary spotting of the genitalia. Halal F Am J Med Genet; 1983 May; 15(1):161. PubMed ID: 6859117 [No Abstract] [Full Text] [Related]
7. [A case of Gardner's syndrome with bilateral epididymis tumors, nasal polyp, bone anomalies and mental deficiency (author's transl)]. Shimizu M; Watanabe K; Yamada M; Watanabe S; Wakahara T Nihon Naika Gakkai Zasshi; 1975 Dec; 64(12):1384-90. PubMed ID: 1240914 [No Abstract] [Full Text] [Related]
8. Cronkhite-Canada syndrome: report of an unusual case. Rubin M; Tuthill RJ; Rosato EF; Cohen S Gastroenterology; 1980 Oct; 79(4):737-41. PubMed ID: 7409393 [TBL] [Abstract][Full Text] [Related]
9. [Case of non-familial digestive polyposis with skin symptoms (case of so-called Cronkhite-Canada syndrome)]. Yoshida H; Fukui I; Takahata J; Okubo K; Sawashige E Saishin Igaku; 1969 Sep; 24(9):1990-9. PubMed ID: 5353806 [No Abstract] [Full Text] [Related]
10. Hamartomatous rectal polyps are common in tuberous sclerosis. Gould SR Ann N Y Acad Sci; 1991; 615():71-80. PubMed ID: 2039169 [TBL] [Abstract][Full Text] [Related]
13. Pigmentary changes in Seckel's syndrome. Fathizadeh A; Soltani K; Medenica M; Lorincz AL J Am Acad Dermatol; 1979 Jul; 1(1):52-4. PubMed ID: 500866 [TBL] [Abstract][Full Text] [Related]
14. Cronkhite-Canada syndrome: report of a case with bacteriologic, immunologic, and electron microscopic studies. Ali M; Weinstein J; Biempica L; Halpern A; Das KM Gastroenterology; 1980 Oct; 79(4):731-6. PubMed ID: 7409392 [TBL] [Abstract][Full Text] [Related]
15. Cronkhite Canada syndrome: report of a case with spontaneous recovery. Viranuvatti V; Damrongsak C; Chainuvati T; Vanasin B; Chandrcharoensin C J Med Assoc Thai; 1981 May; 64(5):261-6. PubMed ID: 7252395 [No Abstract] [Full Text] [Related]
16. Oligoprenia with congenital glaucoma and pigmentary skin abnormalities in two brothers: a new genetic syndrome. Predescu V; Christodorescu D; Costiner E Rev Roum Med; 1974; 12(6):437-9. PubMed ID: 4462205 [No Abstract] [Full Text] [Related]
17. Sotos syndrome in two brothers. Boman H; Nilsson D Clin Genet; 1980 Dec; 18(6):421-7. PubMed ID: 7449180 [TBL] [Abstract][Full Text] [Related]