Multiple Intestinal Neoplasia Caused by a Mutation in the Murine Homolog of the APC Gene

Author:

Su Li-Kuo1,Kinzler Kenneth W.1,Vogelstein Bert1,Preisinger Antonette C.1,Moser Amy Rapaich2,Luongo Cindy23,Gould Karen A.23,Dove William F.23

Affiliation:

1. Molecular Genetics Laboratory, Johns Hopkins University School of Medicine, Baltimore, MD 21231.

2. McArdle Laboratory for Cancer Research, University of Wisconsin-Madison, Madison, WI 53706.

3. Laboratory of Genetics, University of Wisconsin-Madison, Madison, WI 53706.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

Reference26 articles.

1. ASHTONRICKARDT, P.G., HIGH-FREQUENCY OF APC LOSS IN SPORADIC COLORECTAL-CARCINOMA DUE TO BREAKS CLUSTERED IN 5Q21-22, ONCOGENE 4: 1169 (1989).

2. BODMER, W.F., LOCALIZATION OF THE GENE FOR FAMILIAL ADENOMATOUS POLYPOSIS ON CHROMOSOME-5, NATURE 328: 614 (1987).

3. Bulow, S., Familial Adenomatous Polyposis: 109 (1990).

4. DELATTRE, O, MULTIPLE GENETIC ALTERATIONS IN DISTAL AND PROXIMAL COLORECTAL-CANCER, LANCET 2: 353 (1989).

5. GARDNER, E.J., MULTIPLE CUTANEOUS AND SUBCUTANEOUS LESIONS OCCURRING SIMULTANEOUSLY WITH HEREDITARY POLYPOSIS AND OSTEOMATOSIS, AMERICAN JOURNAL OF HUMAN GENETICS 5: 139 (1953).

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