Cryptic intragenic deletion of the SHOX gene in a family with Léri-Weill dyschondrosteosis detected by Multiplex Ligation-Dependent Probe Amplification (MLPA). [electronic resource]

By: Contributor(s): Producer: 20091007Description: 1382-7 p. digitalISSN:
  • 1677-9487
Subject(s): Online resources: In: Arquivos brasileiros de endocrinologia e metabologia vol. 52
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Publication Type: Case Reports; Evaluation Study; Journal Article; Research Support, Non-U.S. Gov't

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