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Trisomy 1q42.3-qter and monosomy 21q22.3-qter associated with ear anomaly, facial dysmorphology, psychomotor retardation, and epilepsy: delineation of a new syndrome
Authors:Tuschl Karin  Fritz Barbara  Herle Marion  Fonatsch Christa  Bodamer Olaf A
Affiliation:Biochemical and Paediatric Genetics, Department of General Paediatrics, University Children's Hospital, Medical University Vienna, Vienna, Austria.
Abstract:
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