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PMID: 677128 Published · ppublish English Journal Article Research Support, U.S. Gov't, Non-P.H.S.

A robust method for the detection of linkage in familial disease.

American journal of human genetics ·Vol. 30 ·No. 3 ·1978-05-00 ·Pages 308-21

Fishman PM, Suarez B, Hodge SE, Reich T

Abstract

A nonparametric method for the detection of critical genes associated with familial disease was presented. The method involves the detection of deviations from expected identity by descent distributions at polymorphic marker loci for affected sib pairs. The method thus avoids the difficulties arising from incomplete penetrance, variable age of onset and other complications present in other forms of linkage analysis. The theoretical properties of method were worked out in detail for two important cases -- that of an incompletely penetrant recessive or incompletely penetrant dominant critical autosomal gene linked to a codominant marker locus. An easily implementable decision rule for the detection of linkage was proposed, and its operating characteristics for a variety of alternative hypothesis were obtained.

MeSH Terms
Genes, Dominant Genes, Recessive Genetic Diseases, Inborn/genetics Genetic Linkage Humans Mathematics Models, Biological Phenotype
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Fishman P M
Suarez B
Hodge S E
Reich T
References (11)
11 references, click to expand
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Article Info
Journal
American journal of human genetics
Abbr.
Am J Hum Genet
ISSN
0002-9297
Published
1978-05-00
Pages
308-21
Language
English
Region
United States
NLM ID
0370475
PMCID
PMC1685584
Subset
IM
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