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Fragile X syndrome: diagnosis using highly polymorphic microsatellite markers.

We describe two highly polymorphic microsatellite AC repeat sequences, VK23AC and VK14AC, which are closely linked to the fragile X at Xq27.3. Both VK23AC (DXS297) and VK14AC (DXS292) are proximal to the fragile site. Two-point linkage analysis in 31 fragile X families gave (a) a recombination frequ...

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Detalhes bibliográficos
Main Authors: Richards, R I, Shen, Y, Holman, K, Kozman, H, Hyland, V J, Mulley, J C, Sutherland, G R
Formato: Artigo
Idioma:Inglês
Publicado em: 1991
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1683096/
https://ncbi.nlm.nih.gov/pubmed/2035525
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