Genetic mapping of new DNA probes at Xq27 defines a strategy for DNA studies in the fragile X syndrome

The fragile X syndrome is the most common cause of familial mental retardation and is characterized by a fragile site at the end of the long arm of the X chromosome. The unusual genetics and cytogenetics of this X-linked condition make genetic counseling difficult. DNA studies were of limited value...

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Main Authors: Suthers, G. K., Mulley, J. C., Voelckel, M. A., Dahl, N., Väisänen, M. L., Steinbach, P., Glass, I. A., Schwartz, C. E., van Oost, B. A., Thibodeau, S. N., Haites, N. E., Oostra, B. A., Giné, R., Carballo, M., Morris, C. P., Hopwood, J. J., Sutherland, G. R.
Formato: Artigo
Idioma:Inglês
Publicado: 1991
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Original Articles
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC1682966/
https://ncbi.nlm.nih.gov/pubmed/1671806
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