ISB-Led Team Publishes Whole-Genome Sequencing Study Involving Family of Four | GenomeWeb

By a GenomeWeb staff reporter

NEW YORK (GenomeWeb News) – Researchers from the Institute for Systems Biology and elsewhere reported in the early, online version of Science last night that they have used whole-genome sequencing to identify mutations behind a Mendelian condition called Miller syndrome and an inherited lung disorder called ciliary dyskinesia in a family of four.

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