Explaining a genetic disorder's unique shift

Findings reported in this week's PLoS Biology give insight into the unique characteristics of the birth defect known as Prader-Willi Syndrome (PWS), and at the same time, may help explain the way that a certain type of gene is expressed in all humans.

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<p><a href="http://www.physorg.com/news138941030.html">Explaining a genetic disorder's unique shift</a></p> <p>Findings reported in this week's <I>PLoS Biology </I>give insight into the unique characteristics of the birth defect known as Prader-Willi Syndrome (PWS), and at the same time, may help explain the way that a certain type of gene is expressed in all humans.</p>