HIGHLIGHTS
- who: design08 from the (UNIVERSITY) have published the Article: Synopses of Research Articles, in the Journal: (JOURNAL)
- what: Study of this activity will likely help illuminate the pathologic mechanism of a rare human developmental disorder, Cornelia de Lange syndrome, which can be caused by a mutation in the delangin gene and which is characterized by low birth weight, slow growth, and multiple physical abnormalities. This study shows the value of using microarrays to home in on likely mediators of regeneration at different stages of the process. The model shows that body temperature increases with body . . .
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