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2. Relationship between variation trinucleotide repeat in Huntington's expansion disease. aNnadtiuprheenotGeynp, iect;Snell, R.G.; MacMillan, J.C.; Cheadle, J.P.; ct al,1993
3. The relationship between trinucleotide (CAG) repeat length and clinical features of Huntington's disease;Andrew, S.E.; Goldberg, Y.P.; Kremer, B.;Natuire Geniet,1993
4. Fragile-X syndrome: Huunmi)qzueGetgieentet1i9c9s2; o5f0:th9e68h-e8r0i.table unstable clement. Am) _7 in fragile X syndrome and HD suggests that 12;Yu, S.; Mulley, J.; Loesch, D.;Cell; Molecular trinucleotide repeat expansion in these two disorders might result from fundamentally different mechanisms. A detailed analysis of repeat instability in each of the other disorders b(aCsTisGo)f mvotonic repeat at dtyhsetr3'opehny:d eoxfpaanstiraonnscorfiapttreinncucoldeiontgidea protein kinase family member,1992
5. Detection of an unstable myotonic fdryasgtmreonpthy.ofNDatNuiAre specific to individuals;Buxton, J.; Shelburne, P.; Davies, J.,1992