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New test scans all genes simultaneously to identify single mutation causing child's rare genetic disease




Sequencing the DNA of children with mystery genetic disorders produced a definitive diagnosis in 40 percent of one hospital’s most complex cases -- a quantum leap from the field’s 5-percent success rate 20 years ago.

Fuente : http://feeds.sciencedaily.com/~r/sciencedaily/~3/K...

Sábado, 18 de Octubre 2014
Jueves, 1 de Enero 1970
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