Segregation analysis of Colorectal-Cancer in Northern Ireland
Segregation analysis of Colorectal-Cancer in Northern Ireland
The genetic basis for colorectal cancer was investigated by complex segregation analysis of a published series of 305 pedigrees ascertained through a large population database. Two hundred and five of the pedigrees were ascertained through patients diagnosed with colorectal cancer before age 55, and 100 from patients diagnosed with colorectal cancer between the ages of 55 and 74. The analysis was carried out using the program POINTER. Using the joint-likelihood approach, the familial aggregation of colorectal cancer was compatible with the inheritance of a dominant gene. The gene frequency of the putative abnormal allele was 0.002 with a lifetime penetrance of 85%. However, under conditional likelihood, this mode of inheritance for a major gene was not favoured. The possible aetiologies of this paradoxical finding are discussed
POLYPS, NONPOLYPOSIS COLON-CANCER, LYNCH SYNDROME-I, COLORECTAL CANCER
41-48
Houlston, Richard S.
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Collins, Andrew
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Kee, Fiona
c732028e-07a5-417d-9339-d3437afe8cf4
Collins, Brendan J.
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Shields, Denis C.
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Morton, Newton Ennis
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1 January 1995
Houlston, Richard S.
513f47bc-c527-47d5-847d-20482ab5d583
Collins, Andrew
7daa83eb-0b21-43b2-af1a-e38fb36e2a64
Kee, Fiona
c732028e-07a5-417d-9339-d3437afe8cf4
Collins, Brendan J.
12196b22-96d3-4a71-82dc-8b4ea380918f
Shields, Denis C.
57ffee4f-0277-4b3d-9c7a-8c328637d8e6
Morton, Newton Ennis
c668e2be-074a-4a0a-a2ca-e8f51830ebb7
Houlston, Richard S., Collins, Andrew, Kee, Fiona, Collins, Brendan J., Shields, Denis C. and Morton, Newton Ennis
(1995)
Segregation analysis of Colorectal-Cancer in Northern Ireland.
Human Heredity, 45 (1), .
(doi:10.1159/000154253).
Abstract
The genetic basis for colorectal cancer was investigated by complex segregation analysis of a published series of 305 pedigrees ascertained through a large population database. Two hundred and five of the pedigrees were ascertained through patients diagnosed with colorectal cancer before age 55, and 100 from patients diagnosed with colorectal cancer between the ages of 55 and 74. The analysis was carried out using the program POINTER. Using the joint-likelihood approach, the familial aggregation of colorectal cancer was compatible with the inheritance of a dominant gene. The gene frequency of the putative abnormal allele was 0.002 with a lifetime penetrance of 85%. However, under conditional likelihood, this mode of inheritance for a major gene was not favoured. The possible aetiologies of this paradoxical finding are discussed
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Published date: 1 January 1995
Keywords:
POLYPS, NONPOLYPOSIS COLON-CANCER, LYNCH SYNDROME-I, COLORECTAL CANCER
Identifiers
Local EPrints ID: 470496
URI: http://eprints.soton.ac.uk/id/eprint/470496
ISSN: 0001-5652
PURE UUID: 5c09c0ba-870b-44cb-af9a-33bb876c2913
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Date deposited: 11 Oct 2022 17:01
Last modified: 17 Mar 2024 02:37
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Author:
Richard S. Houlston
Author:
Fiona Kee
Author:
Brendan J. Collins
Author:
Denis C. Shields
Author:
Newton Ennis Morton
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