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Perinatal findings and molecular cytogenetic analysis of de novo partial trisomy 16q (16q22.1→qter) and partial monosomy 20q (20q13.3→qter)
Authors:Chih-Ping Chen  Shuan-Pei Lin  Chyi-Chyang Lin  Yueh-Chun Li  Schu-Rern Chern  Wei-Min Chen  Chen-Chi Lee  Lie-Jiau Hsieh  Wayseen Wang
Affiliation:1. Department of Obstetrics and Gynecology, Mackay Memorial Hospital, Taipei, Taiwan, Republic of China;2. Department of Medical Research, Mackay Memorial Hospital, Taipei, Taiwan, Republic of China

Department of Pediatrics, Mackay Memorial Hospital, Taipei, Taiwan, Republic of China;3. Department of Medical Genetics, China Medical University Hospital, Taichung, Taiwan, Republic of China;4. Department of Life Sciences, Chung-Shan Medical University, Taichung, Taiwan, Republic of China;5. Department of Medical Research, Mackay Memorial Hospital, Taipei, Taiwan, Republic of China;6. Department of Obstetrics and Gynecology, West-Garden Hospital, Taipei, Taiwan, Republic of China

Abstract:
Keywords:chromosome 20q deletion  FISH  partial trisomy 16q  polymorphic DNA marker analysis  SKY
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