Non-random asynchronous replication at 22q11.2 favours unequal meiotic crossovers leading to the human 22q11.2 deletion. [electronic resource]

By: Contributor(s): Producer: 20040927Description: 413-20 p. digitalISSN:
  • 1468-6244
Subject(s): Online resources: In: Journal of medical genetics vol. 41
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't

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