Fragile X syndrome: genetic localisation by linkage mapping of two microsatellite repeats FRAXAC1 and FRAXAC2 which immediately flank the fragile site.

We report the genetic localisation of the fragile site at Xq27.3 associated with fragile X syndrome. The position of the fragile site within the multipoint linkage map was determined using two polymorphic microsatellite AC repeat markers FRAXAC1 and FRAXAC2. These markers were physically located wit...

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Autori principali: Richards, R I, Holman, K, Kozman, H, Kremer, E, Lynch, M, Pritchard, M, Yu, S, Mulley, J, Sutherland, G R
Natura: Artigo
Lingua:Inglês
Pubblicazione: 1991
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Research Article
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC1017157/
https://ncbi.nlm.nih.gov/pubmed/1757956
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