1Blair NP,Trempe CL.Hypertrophy of the retinal pigment epithelium associated with Gardner's syndrome[J].Am J Ophthalmol,1980,90:661-667.
2Kurz GH,Zimmerman LE.Vagaries of the retinal pigment epithelium[J].Int Ophthalmol Clin,1962,2:441.
3Reese AB,Jones IS.Benign melanomas of the retinal pigment epithelium[J].Am J Ophthalmol,1956,42:207-212.
4Aiello LP,Traboulsi EI.Pigmented fundus lesions in a preterm infant with familial adenomatous polyposis[J].Arch Ophthalmol,1993,111:302-303.
5Traboulsi EI,Murphy SF,de la Cruz ZC,et al.A clinicopathologic study of the eyes in familial adenomatous polyposis with extracolonic manifestations (Gardner' s syndrome)[J].Am J Ophthalmol,1990,110:550-561.
6Baba S,Tsuchiya M,Watanabe I,et al.Importance of retinal pigmentation as a subclinical marker in familial adenomatous polyposis[J].Dis Colon Rectum,1990,33:660-665.
7Polkinghorne PJ,Ritchie S,Neale K,et al.Pigmented lesions of the retinal pigment epithelium and familial adenomatous polyposis[J].Eye,1990,4:216-221.
8Giardiello FM,Petersen GM,Piantadosi S,et al.APC gene mutations and extraintestinal phenotype of familial adenomatous polyposis[J].Gut,1997,40:521-525.
10Wallis YL,Macdonald F,Hultén M,et al.Genotypephenotype correlation between position of constitutional APC gene mutation and CHRPE expression in familial adenomatous polyposis[J].Hum Genet,1994,94:543-548.
2Wang Z J, Churchman M, Avizienyte E, et al. Germline mutations of the LKB1 (STKll) gene in Peutz-Jeghers pa- tients[J]. J Med Genet, 1999,36(5) :365-368.
4Wang Z J, Churchman M, Avizienyte E, et al. Germline mutations of the LKB1 (STKll) gene in Peutz-Jeghers pa- tients[J]. J Med Genet, 1999,36(5) :365-368.
