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FG syndrome: Linkage analysis in two families supporting a new gene localization at Xp22.3 [FGS3]
Authors:Marie Pierre Moizard  Jean Louis Gilardi  John M. Opitz  Helen Middleton‐Price  Marcus Pembrey  Claude Moraine  Sylvain Briault
Affiliation:1. Service de Génétique, CHU Bretonneau, Tours, France;2. INSERM U316, CHU Bretonneau, Tours, France;3. Departments of Pediatrics (Medical Genetics), Human Genetics, Obstetrics and Gynecology, University of Utah, Salt Lake City, Utah;4. Institute of Child Health, University of London, London, England
Abstract:
Keywords:FG syndrome  FGS1  FGS2  FGS3  Xp22.3  linkage analysis  VCX‐A  PRKX
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