RFLP FOR LINKAGE ANALYSIS OF FRAGILE X SYNDROME
Author:
Publisher
Elsevier BV
Subject
General Medicine
Reference10 articles.
1. Conference report. Second International Workshop on the Fragile X and on X-linked Mental Retardation;Turner;Am J Med Genet,1986
2. Polymorphic DNA markers in prenatal diagnosis of fragile X syndrome;Oberle;Lancet,1985
3. First trimester prenatal diagnosis of a male fetus with fragile X;Tommerup;Lancet,1985
4. Close linkage of fragile X linked mental retardation syndrome to haemophilia B and transmission through a normal male;Camerino;Nature,1983
5. The telomeric region of the human C chromosome long arm. Presence of a highly polymorphic DNA marker and analysis of recombination frequency;Oberle;Proc Natl Acad Sci USA,1985
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1. Diagnostic molecular genetics of the fragile X;Clinical Genetics;2008-06-28
2. The fragile X Syndrome;Molecular Genetic Medicine;1992
3. Techniques of Molecular Biology;A Primer of Molecular Biology;1992
4. Premutation for the Martin-Bell syndrome analyzed in a large pedigree segregating also for G6PD-deficiency. I: A working hypothesis on the nature of the FRAX-mutations;American Journal of Medical Genetics;1991-09-15
5. New polymorphism and a new chromosome breakpoint establish the physical and genetic mapping of DXS369 in the DXS98-FRAXA Interval;American Journal of Medical Genetics;1991-02-01
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