𝔖 Bobbio Scriptorium
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Introductory comments—Special section: Prader–Willi syndrome

✍ Scribed by John C. Carey


Publisher
John Wiley and Sons
Year
2007
Tongue
English
Weight
58 KB
Volume
143A
Category
Article
ISSN
1552-4825

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Introductory comments on special section
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## Abstract The clinical implementation of array‐based comparative genomic hybridization (aCGH) has allowed detection of copy number variations (CNVs) from megabases in size to those involving only a single exon. One major challenge that followed the clinical implementation of array CGH technology