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  • Molecular assay reagents intended for use in identifying deletions in chromosome 22 band q13.3. These genetic deletions are present in patients with a disorder that may be the result of a de novo chromosome deletion or of an inherited chromosome abnormality, characterized by neonatal hypotonia, normal-to-accelerated growth, absent or delayed speech, and anatomic abnormalities (e.g., face, hands, toenails).
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