Use of robust statistical methods to determine the effect of fragile X on means and variance components of a quantitative trait
- 1 January 1995
- journal article
- research article
- Published by Wiley in Genetic Epidemiology
- Vol. 12 (3) , 279-290
- https://doi.org/10.1002/gepi.1370120305
Abstract
Owing to the presence of outliers, an estimated 3.5% in the ridge breadth data and 1.7% in the height data, the effect of fragile X on height and ridge breadth was examined using robust statistical techniques for data collected from 54 families afflicted with this disorder. It is shown that fragile X affects ridge breadth and height in a different manner. Fragile X women had a greater mean ridge breadth than normal women, whereas there was a similar trend, but no significant difference, between normal and fragile X men. Fragile X men were shorter than normal men, but no significant difference between the mean height of normal and fragile X women was observed. However, fragile X girls were shown to grow more quickly and to stop growing earlier than normal girls. An examination of the covariance between relatives classified according to fragile X status showed that for both traits the effect of fragile X was to reduce the covariance between parents and offspring, which produced the effect of departure from an additive polygenic model of inheritance. ©1995 Wiley‐Liss, Inc.Keywords
This publication has 23 references indexed in Scilit:
- APPLICATIONS OF ROBUST ESTIMATION FOR VARIANCE COMPONENTS MODELS:THE DETECTION OF MAJOR GENE EFFECTS IN FINGER RIDGE COUNTS IN NORMAL AND FRAGILE X FAMILIESAustralian Journal of Statistics, 1994
- Effect of fragile X on physical and intellectual traits estimated by pedigree analysisAmerican Journal of Medical Genetics, 1993
- Genetic and environmental contributions to the variance of body height in a sample of first and second degree relativesAmerican Journal of Physical Anthropology, 1992
- Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradoxCell, 1991
- Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndromePublished by Elsevier ,1991
- Clinical features and reproductive patterns in fragile X female heterozygotes.Journal of Medical Genetics, 1988
- Anthropometry in Martin‐Bell syndromeAmerican Journal of Medical Genetics, 1988
- Dermatoglyphic findings in fragile X syndrome: a causal hypothesis points to X-Y interchangeAnnals of Human Genetics, 1986
- Longitudinal data analysis using generalized linear modelsBiometrika, 1986
- Use of robust variance components models to analyse triglyceride data in familiesAnnals of Human Genetics, 1985