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