Linkage heterogeneity and fragile X
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Link
http://link.springer.com/content/pdf/10.1007/BF00291731.pdf
Reference34 articles.
1. Brown WT, Gross AC, Chan CB, Jenkins EC (1986) DNA linkage studies in the fragile X syndrome suggest genetic heterogeneity. Am J Med Genet 23:643?665
2. Brown WT, Jenkins EC, Gross AC, Chan CB, Krawczun MS, Duncan CJ, Sklower SL, Fisch GS (1987) Further evidence for genetic heterogeneity in the fragile X syndrome. Hum Genet 75:311?321
3. Buchanan JA, Buckton KE, Gosden CM, Newton MS, Clayton JF, Christie S, Hastie NH (1987) Ten families with fragile X syndrome: linkage relationships with four DNA probes from distal Xq. Hum Genet 76:165?172
4. Camerino G, Mattei MG, Mattei JF, Jaye M, Mandel JL (1983) Close linkage of fragile X-mental retardation syndrome to haemophilia B and transmission through a normal male. Nature 306:701?704
5. Choo KH, George D, Filby D, Halliday JL, Leversha M, Webb G, Danks DM (1984) Linkage analysis of X-linked mental retardation with and without fragile-X factor IX gene probe. Lancet II:349
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3. Linkage homogeneity near the fragile X locus in normal and fragile X families;Genomics;1991-07
4. Bibliography on X-linked mental retardation, the fragile X, and related subjects V (1991);American Journal of Medical Genetics;1991-02-01
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