๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

COLORECTAL DISEASES: COMMENT

โœ Scribed by Peter B. Loder


Book ID
108994421
Publisher
John Wiley and Sons
Year
1998
Tongue
English
Weight
99 KB
Volume
68
Category
Article
ISSN
1445-1433

No coin nor oath required. For personal study only.


๐Ÿ“œ SIMILAR VOLUMES


COLORECTAL DISEASES: REPLY
โœ William H. Isbister ๐Ÿ“‚ Article ๐Ÿ“… 1998 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 56 KB
Comment on โ€œAscertainment adjustment in
โœ Michael P. Epstein ๐Ÿ“‚ Article ๐Ÿ“… 2002 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 73 KB

Glidden and Liang [2002] have raised important issues regarding ascertainment adjustment in the framework of variance-components modeling for complex genetic traits. While the structure of the authors' logistic variance-component model is simple, ascertainment issues arising with this model are like

Comment on โ€œAscertainment adjustment in
โœ Paul R. Burton ๐Ÿ“‚ Article ๐Ÿ“… 2002 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 66 KB

The complex diseases continue to provide new challenges for genetic epidemiology. In the current edition of Genetic Epidemiology, Glidden and Liang [2002] consider the effect of latent heterogeneity in disease risk on ascertainmentadjusted parameter estimates, particularly in variance components mod

Genetic linkage and complex diseases: A
โœ R. C. Elston; A. F. Wilson ๐Ÿ“‚ Article ๐Ÿ“… 1990 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 191 KB

Results from the study by Sherrington et a]. [1988] indicate that the maximum lod score (3.2) from a linkage analysis between narrowly defined clinical diagnostic criteria for schizophrenia and polymorphic markers on chromosome 5 is lower than that (6.5) from an analogous analysis between broadly de

Genetic linkage and complex diseases: A
โœ Philip Green ๐Ÿ“‚ Article ๐Ÿ“… 1990 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 211 KB

For diseases with a complex mode of inheritance, such as schizophrenia, traditional linkage analysis assuming Mendelian inheritance of a single gene may be expected to have relatively low power, but to occasionally detect (in fortuitous pedigree samples) either a rare gene which by itself causes the