Novel mutation in the tyrosine kinase domain of FGFR2 in a patient with Pfeiffer syndrome. [electronic resource]

By: Contributor(s): Producer: 20050411Description: 299-300 p. digitalISSN:
  • 1552-4825
Subject(s): Online resources: In: American journal of medical genetics. Part A vol. 131
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Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't

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