DNA linkage studies in the fragile X syndrome suggest genetic heterogeneity
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference15 articles.
1. (1985): Genetic linkage heterogeneity in the fragile X syndrome. Human Genetics. In Press.
2. Close linkage of fragile X-mental retardation syndrome to haemophilia B and transmission through a normal male
3. LINKAGE ANALYSIS OF X-LINKED MENTAL RETARDATION WITH AND WITHOUT FRAGILE-X USING FACTOR IX GENE PROBE
4. Linkage studies of X-linked mental retardation: High frequency of recombination in the telomeric region of the human X chromosome (fragile site/linkage/recombination/X chromosome)
5. Cloning of a representative genomic library of the human X chromosome after sorting by flow cytometry
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1. Transmission of the fra(X) haplotype from three nonpenetrant brothers to their affected grandsons;American Journal of Medical Genetics;1992-06-01
2. Fifth international workshop on the fragile X and X-linked mental retardation;American Journal of Medical Genetics;1992-04-15
3. The fragile X Syndrome;Molecular Genetic Medicine;1992
4. Problems in ascertainment of transmitting males in Martin-Bell syndrome;American Journal of Medical Genetics;1991-12-15
5. Linkage homogeneity near the fragile X locus in normal and fragile X families;Genomics;1991-07
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