Combined use of molecular and biomarkers for presymptomatic carrier risk assessment in familial adenomatous polyposis:

Author:

Bapat Bharati V.,Parker John A.,Berk Theresa,Cohen Zane,McLeod Robin S.,Ray Peter N.,Stern Hartley S.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Gastroenterology,General Medicine

Reference42 articles.

1. Bussey HJ. Familial polyposis coli. Family studies, histopathology, differential diagnosis, and results of treatment. Baltimore: Johns Hopkins University Press, 1975.

2. Gardner EJ, Richards RC. Multiple cutaneous and subcutaneous lesions occurring simultaneously with hereditary polyposis and osteomatosis. Am J Human Genet 1953;5:139–47.

3. Traboulsi EI, Krush AJ, Gardner EJ,et al. Prevalence and importance of pigmented ocular fundus lesions in Gardner's syndrome. N Engl J Med 1987;316:661–7.

4. Blair NP, Trempe CL. Hypertrophy of the retinal pigment epithelium associated with Gardner's syndrome. Am J Ophthalmol 1980;90:661–7.

5. Leppard BJ, Bussey HJ. Epidermoid cysts, polyposis coli and Gardner's syndrome. Br J Surg 1975;62:387–93.

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