References
- Gardner E J, Richards R C. Multiple cutaneous and subcutaneous lesions occurring simultaneously with hereditary polyposis and osteomatosis. Am J Hum Genet 1953; 5: 139–147
- Gardner E J. Follow-up study of a family group exhibiting dominant inheritance for a syndrome including intestinal polyps, osteomas, fibromas and epidermal cysts. Am J Hum Genet 1962; 14: 376–390
- McKittrick L S, Talbott J H, Mallory TB, et al. Case records of the Massachusetts General Hospital: case 21061. N Engl JMed 1935; 212: 263–267
- Blair N P, Trempe C L. Hypertrophy of the retinal pigment epithelium associated with Gardner's syndrome. Am J Ophthalmol 1980; 90: 661–667
- Berk T, Cohen Z, McLeod R S, Parker J A. Congenital hypertrophy of the retinal pigment epithelium as a marker for familial adenomatous polyposis. Dis Colon Rectum 1988; 31: 253–257
- Baker R H, Heinemann M H, Miller H H, De Cosse J J. Hyperpigmented lesions of the retinal pigment epithelium in familial adenomatous polyposis. Am J Med Genet 1988; 31: 427–435
- Chapman P D, Church W, Burn J, Gunn A. Congenital hypertrophy of the retinal pigment epithelium; a sign of familial adenomatous polyposis. Br Med J 1989; 298: 352–354
- Romania A, Zakov N, McGannon E, et al. Congenital hypertrophy of the retinal pigment epithelium in familial adenomatous polyposis. Ophthalmology 1989; 96: 879–884
- Polkinghorne P J, Ritchie S, Neale K, et al. Pigmented lesions of the retinal pigment epithelium and familial adenomatous polyposis. Eye 1990; 4: 216–222
- Burn J, Chapman P, Delhanty J, et al. The UK Northern Region genetic register for familial adenomatous polyposis coli: use of age of onset, congenital hypertrophy of the retinal pigment epithelium, and DNA markers in risk calculation. J Med Genet 1991; 28: 289–296
- Traboulsi E I, Maumenee I H, Krush AJ, et al. Pigmented ocular fundus lesions in the inherited gastrointestinal polyposis syndromes and in hereditary non polyposis colorectal cancer. Ophthalmology 1988; 95: 964–969
- Gass J DM. Retinal and pigment epithelial hamartomas. Stereoscopic Atlas of Macular Disorders, JDM Glass. Mosby Co, St Louis 1987; 605–652
- Bodmer W F, Bailey C J, Bodmer J, et al. Localisation of the gene for familial adenomatous polyposis on chromosome 5. Nature 1987; 328: 614–619
- Kinzler K, Nilbert M C, Su LK, et al. Identification of FAP locus genes from chromosome 5q21. Science 1991; 253: 661–664
- Groden J, Thliveris A, Samowitz W, et al. Identification and characterisation of the familial adenomatous polyposis coli gene. Cell 1991; 66: 589–600