Characterisation of variant alleles at the HumD21S11 locus implies unique Australasian genotypes and re-classification of nomenclature guidelines
Author:
Publisher
Elsevier BV
Subject
Pathology and Forensic Medicine,Law
Reference29 articles.
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3. High resolution of human evolutionary trees with polymorphic microsatellites;Bowcock;Nature,1994
4. Familial Alzheimer’s disease (FAD): co-segregation between alleles at the D21S11 DNA marker and the FAD gene in a particular pedigree;David;J. Neurol.,1988
5. Allelic variability in D21S11, but not in APP or APOE, is associated with cognitive decline in Down syndrome;Farrer;NeuroReport,1997
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