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Sharing of genetic data empowers discovery of new disorders in children

from Medical Xpress

The team behind the Deciphering Developmental Disorders Study, one of the world's largest nationwide rare disease genome-wide sequencing initiatives, have developed a novel computational approach to identify genetic variants that cause disease in young children. This approach is only made possible by contrasting the DNA of children with severe developmental disorders of unknown genetic cause, with the DNA from individuals without overt developmental disorders. more


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