Literature DB >> 6690013

Failure to demonstrate a chromosome 2 deletion in adenomatous colorectal polyposis patients.

R M Fineman, M Morgan, R W Burt, E J Gardner.   

Abstract

A group of researchers recently reported a specific chromosome abnormality consisting of a deletion in the long arm (q) of chromosome 2 in patients with adenomatous colorectal polyposis. Using a high resolution chromosome banding technique and a blind study design, the authors karyotyped two patients with Gardner syndrome, two patients with familial polyposis, and four normal controls. No deletion was found in chromosome 2.

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Year:  1984        PMID: 6690013     DOI: 10.1002/1097-0142(19840115)53:2<317::aid-cncr2820530223>3.0.co;2-c

Source DB:  PubMed          Journal:  Cancer        ISSN: 0008-543X            Impact factor:   6.860


  2 in total

1.  A genetic study of Gardner syndrome and congenital hypertrophy of the retinal pigment epithelium.

Authors:  L A Lyons; R A Lewis; L C Strong; S Zuckerbrod; R E Ferrell
Journal:  Am J Hum Genet       Date:  1988-02       Impact factor: 11.025

2.  Comparison of radiation-induced chromosomal damage between normal individuals and patients with familial polyposis coli.

Authors:  S Kakati; L Herrera; R E Drury; A A Sandberg
Journal:  J Cancer Res Clin Oncol       Date:  1988       Impact factor: 4.553

  2 in total

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