Výsledky vyhledávání - "Laura J. Ward"

The Kell blood group locus is close to the cystic fibrosis locus on chromosome 7

Autor: Laura J. Ward, James L. Weber, Kavita R. Purohit, Bronya J.B. Keats

Publikováno v: Human Genetics. 89

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::13bdae9d5aa303c8e747ef4acb07b17d
https://doi.org/10.1007/bf00194323

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Gametic equilibrium between 24 polymorphic markers

Autor: Jaime L. Hernández, Robert C. Elston, Laura J. Ward

Publikováno v: Human Genetics. 85

Pairs of unlinked genetic markers (blood cell antigens and enzymes and serum proteins) were tested for gametic equilibrium (GE) in data from 508 unrelated individuals from different regions of North America. A total of 24 markers were considered in t

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::521dea816b4008e100d39a5d94c658b9
https://doi.org/10.1007/bf00206759

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Linkage and segregation analyses of apolipoproteins A1 and B, and lipoprotein cholesterol levels in a large pedigree with excess coronary heart disease: The Bogalusa heart study

Autor: Christopher I. Amos, Robert C. Elston, Sathanur R. Srinivasan, Alexander F. Wilson, James L. Cresanta, Laura J. Ward, Gerald S. Berenson, D. C. Rao

Publikováno v: Genetic Epidemiology. 4:115-128

Robust methods were employed, using data from a single large pedigree, to screen serum apolipoprotein A1 and B levels, serum lipoprotein cholesterol levels, and ratios of serum lipoprotein cholesterol fractions to apolipoprotein A1 and B levels for g

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::6fb274d26263e6e176644d99d2a13f0a
https://doi.org/10.1002/gepi.1370040206

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Association between polymorphic blood markers and risk factors for cardiovascular disease in a large pedigree

Autor: Varghese T. George, Robert C. Elston, Chris I. Amos, Laura J. Ward, Gerald S. Berenson, D. C. Rao

Publikováno v: Genetic Epidemiology. 4:267-275

A large pedigree with high prevalence of heart disease is investigated to analyse the association between polymorphic blood markers and quantitative risk factors for cardiovascular disease. The analysis incorporates a familial correlation structure a

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::75dcda5f31174be5f2e390ec4717d509
https://doi.org/10.1002/gepi.1370040405

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Linkage relationships between a major gene for catechol-o-methyltransferase activity and 25 polymorphic marker systems

Autor: Robert C. Elston, Richard M. Weinshilboum, Laura J. Ward, Alexander F. Wilson, Roger M. Siervogel

Publikováno v: American Journal of Medical Genetics. 19:525-532

Segregation analysis has provided evidence suggesting the existence of a major gene for catechol-o-methyltransferase (COMT) activity in man. Five large families (4 Caucasian, 1 black), with a total of 1,189 individuals, were ascertained as part of a

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e1277b120a1ce6e9bdb88a95e3f69a6b
https://doi.org/10.1002/ajmg.1320190314

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'Acadian' and 'classical' forms of Friedreich ataxia are most probably caused by mutations at the same locus

Autor: Jacqui Shaw, Laura J. Ward, Aranda Wickremasinghe, Susan Chamberlain, Bronya J.B. Keats

Publikováno v: American Journal of Medical Genetics. 33:266-268

"Acadian ataxia" is a form of Friedreich ataxia found in individuals of Acadian ancestry. It was described by Barbeau (in Sobue I (ed): Spinocerebellar Degeneration; Tokyo: Univ. Tokyo Press, pp 121-142, 1980) as having a slower course of degeneratio

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2e250748f1a9393ceb01afe3875ea50c
https://doi.org/10.1002/ajmg.1320330224

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