Autosomal suppressor gene for fragile-X: An hypothesis
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference14 articles.
1. Inheritance of fragile X syndrome: An hypothesis
2. Normal male carriers in the fra(X) form of X-linked mental retardation (Martin—Bell syndrome)
3. The female and the Fragile X. A study of 144 obligate female carriers
4. (1983): The heterozygous female. In (eds): “The Fragile X Syndrome: Diagnosis, Biochemistry and Intervention”. Dillon, Colorado: Spectra Publishing Co. Inc., pp 83-;94.
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2. The Inheritance of Left-Handedness;Ciba Foundation Symposium 162 - Biological Asymmetry and Handedness;2007-09-28
3. Evolving Methods in Genetic Epidemiology. IV. Approaches to Non-Mendelian Inheritance;Epidemiologic Reviews;1997-01-01
4. Predictions of a 2-locus model for disease heterogeneity: Application to adrenoleukodystrophy;American Journal of Medical Genetics;1992-11-15
5. Population genetics of the fragile-X syndrome: multiallelic model for the FMR1 locus.;Proceedings of the National Academy of Sciences;1992-05-01
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