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檢索結果筆數(5)。
各著作權人授權國家圖書館,敬請洽詢 nclper@ncl.edu.tw
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題 名:
Familial Transmission of Recurrent 15q11.2 (BP1-BP2) Microdeletion Encompassing NIPA1, NIPA2, CYFIP1, and TUBGCP5 Associated with Phenotypic Variability in Developmental, Speech, and Motor Delay:
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作 者:
Chen, Chih-ping;
Lin, Shuan-pei;
Lee, Chung-lin;
Chern, Schu-rern;
Wu, Peih-shan;
Chen, Yen-ni;
Chen, Shin-wen;
Wang, Wayseen;
- 書刊名:
Taiwanese Journal of Obstetrics & Gynecology
- 卷 期:
56:1 2017.02[民106.02]
- 頁 次:
頁93-97
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被引用次數:期刊(0) 博士論文(0) 專書(0) 專書論文(0)
排除自我引用:0
共同引用:0
點閱:0
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題 名:
Recurrent 2q13 Microduplication Encompassing MALL, NPHP1, RGPD6, and BUB1 Associated with Autism Spectrum Disorder, Intellectual Disability, and Liver Disorder:
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作 者:
Chen, Chih-ping;
Lin, Shuan-pei;
Lee, Chung-lin;
Chern, Schu-rern;
Wu, Peih-shan;
Chen, Yen-ni;
Chen, Shin-wen;
Wang, Wayseen;
- 書刊名:
Taiwanese Journal of Obstetrics & Gynecology
- 卷 期:
56:1 2017.02[民106.02]
- 頁 次:
頁98-101
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被引用次數:期刊(0) 博士論文(0) 專書(0) 專書論文(0)
排除自我引用:0
共同引用:0
點閱:0
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題 名:
Molecular Cytogenetic Characterization and Prenatal Diagnosis of Familial Xp22.33 Microdeletion Encompassing Short Stature Homeobox Gene in a Male Fetus with a Favorable Outcome:
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作 者:
Chen, Chih-ping;
Ko, Tsang-ming;
Wang, Liang-kai;
Lin, Shuan-pei;
Chern, Schu-rern;
Wu, Peih-shan;
Chen, Yen-ni;
Chen, Shin-wen;
Yang, Chien-wen;
Town, Dai-dyi;
Lee, Meng-shan;
Wang, Wayseen;
- 書刊名:
Taiwanese Journal of Obstetrics & Gynecology
- 卷 期:
56:2 2017.04[民106.04]
- 頁 次:
頁264-267
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被引用次數:期刊(0) 博士論文(0) 專書(0) 專書論文(0)
排除自我引用:0
共同引用:0
點閱:0
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題 名:
Pfeiffer Syndrome with FGFR2 C342R Mutation Presenting Extreme Proptosis, Craniosynostosis, Hearing Loss, Ventriculomegaly, Broad Great Toes and Thumbs, Maxillary Hypoplasia, and Laryngomalacia:
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作 者:
Chen, Chih-ping;
Lin, Shuan-pei;
Liu, Yu-peng;
Chern, Schu-rern;
Chen, Shin-wen;
Lai, Shih-ting;
Wang, Wayseen;
- 書刊名:
Taiwanese Journal of Obstetrics & Gynecology
- 卷 期:
56:3 2017.06[民106.06]
- 頁 次:
頁412-414
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被引用次數:期刊(0) 博士論文(0) 專書(0) 專書論文(0)
排除自我引用:0
共同引用:0
點閱:0