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Concomitant 11p15.4‐p15.5 duplication and terminal 22q13.33 deletion in a patient with features of Beckwith–Wiedemann syndrome
Authors:Jess F. Peterson  David P. Bick  Gabrielle C. Geddes  Julie McCarrier  John W. Grignon Jr  Brett Chirempes  Ulrich Broeckel  Fatima Abidi  Richard C. Rogers  Luigi Boccuto  Barbara DuPont  Peter vanTuinen
Affiliation:1. Department of Pathology, Medical College of Wisconsin, Milwaukee;2. Wisconsin Diagnostic Laboratories, Milwaukee;3. Correspondence to:;4. Jess F. Peterson, M.D., Department of Pathology, Medical College of Wisconsin, Froedtert/MCW Laboratory Building, 9200 W Wisconsin Ave, Milwaukee, WI 53226. E‐mail:;5. Department of Pediatrics, Section of Genetics, Medical College of Wisconsin, Milwaukee;6. Advanced Genomics Laboratory, Children's Hospital of Wisconsin, Milwaukee;7. Department of Pediatrics, Section of Genomic Pediatrics, Medical College of Wisconsin, Milwaukee;8. Greenwood Genetic Center, Greenwood
Abstract:
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