Article
Refinement of the critical region in a new 7p22.1 microduplication syndrome including craniofacial dysmorphism and speech delay.
American journal of medical genetics. Part A - 1 Nov 2014
Pebrel-Richard Celine, Rouzade Charles, Kemeny Stephan, Eymard-Pierre Eleonore, Gay-Bellile Mathilde, Gouas Laetitia, Tchirkov Andreï, Goumy Carole, Vago Philippe
Abstract excerpt
No abstract is available from the source.
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
