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Perinatal findings and molecular cytogenetic analyses of de novo interstitial deletion of 9q (9q22.3→q31.3) associated with Gorlin syndrome
Authors:Chih-Ping Chen  Shuan-Pei Lin  Tzu-Hao Wang  Yann-Jang Chen  Ming Chen  Wayseen Wang
Institution:1. Department of Obstetrics and Gynecology, Mackay Memorial Hospital, Taipei, Taiwan;2. Department of Medical Research, Mackay Memorial Hospital, Taipei, Taiwan

Department of Pediatrics, Mackay Memorial Hospital, Taipei, Taiwan;3. Department of Obstetrics and Gynecology, Lin-Kou Medical Center, Chang-Gung Memorial Hospital, Chang-Gung University Tao-Yuan, Taiwan;4. Faculty of Life Sciences and Institute of Genome Sciences, National Yang-Ming University, Taipei, Taiwan

Department of Pediatrics, Veteran General Hospital, Taipei, Taiwan;5. Department of Obstetrics and Gynecology, and Center for Medical Genetics, Changhua Christian Hospital, Changhua, Taiwan;6. Department of Medical Research, Mackay Memorial Hospital, Taipei, Taiwan

Abstract:
Keywords:array comparative genomic hybridization (CGH)  fluorescence in situ hybridization (FISH)  Gorlin syndrome  interstitial deletion of 9q  maternal serum screening  PTCH gene
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