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教育部委託研究計畫 計畫執行:國立臺灣大學圖書館
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"peih shan wu"的相關文件
顯示項目 36-45 / 49 (共5頁)
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| 中國醫藥大學 |
2013-06 |
Prenatal diagnosis and molecular cytogenetic characterization of a de novo interstitial deletion of 7q (7q22.1->q31.1)
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陳持平(Chih-Ping Chen)*;(Shing-Jyh Chang,);(Schu-Rern Chern);(Peih-Shan Wu);(Yu-Ting Chen);(Jun-Wei Su);(Wen-Lin Chen);(Wayseen Wang) |
| 中國醫藥大學 |
2013-06 |
Ring chromosome 21 presenting with sacrococcygeal teratoma: prenatal diagnosis, molecular cytogenetic characterization and literature review
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陳持平(Chih-Ping Chen)*;(Po-Jen Cheng);(Shuenn-Dyh Chang);(Yi-Xuan Lee);(Jin-Chung Shih);(Schu-Rern Chern);(Peih-Shan Wu);(Jun-Wei Su);(Adam Hwa-Ming Hsieh);(Teresa Hsiao-Tien Chen);(Li-Feng Chen);(Wayseen Wang) |
| 中國醫藥大學 |
2013-06 |
A boy with cleft palate, hearing impairment, microcephaly, micrognathia and psychomotor retardation and a microdeletion in 6p25.3 involving the DUSP22 gene
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陳持平(Chih-Ping Chen)*;(Shuan-Pei Lin);(Schu-Rern Chern);(Peih-Shan Wu);(Jun-Wei Su);(Wayseen Wang) |
| 中國醫藥大學 |
2013-04 |
Prenatal diagnosis of ring chromosome 2 with lissencephaly and 2p25.3 and 2q37.3 microdeletions detected using array comparative genomic hybridization
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陳持平(Chih-Ping Chen)*;(Chen-Ju Lin);(Tung-Yao Chang);(Schu-Rern Chern);(Peih-Shan Wu);(Yu-Ting Chen);(Jun-Wei Su);(Chen-Chi Lee);(Li-Feng Chen);(Wayseen Wang) |
| 亞洲大學 |
2013-03 |
Prenatal diagnosis and molecular cytogenetic characterization of de novo partial trisomy 12q (12q24.21->qter) and partial monosomy 6q (6q27->qter) associated with coarctation of the aorta, ventriculomegaly and thickened nuchal fold
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陳持平;Chen, Chih-Ping;Yi-Yung Chen;Schu-Rern Chern;Peih-Shan Wu;Jun-Wei Su;Yu-Ting Chen;Li-Feng Chen;Wayseen Wang |
| 中國醫藥大學 |
2013-03 |
Prenatal diagnosis of partial trisomy 3q (3q27.3->qter) and partial monosomy 14q (14q31.3->qter) of paternal origin associated with fetal hypotonia, arthrogryposis, scoliosis and hyperextensible joints
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陳持平(Chih-Ping Chen)*;(Yao-Lung Chang);(Schu-Rern Chern);(Peih-Shan Wu);(Jun-Wei Su);(Wen-Lin Chen);(Li-Feng Chen);(Wayseen Wang) |
| 中國醫藥大學 |
2013-03 |
Prenatal diagnosis and molecular cytogenetic characterization of de novo partial trisomy 12q (12q24.21->qter) and partial monosomy 6q (6q27->qter) associated with coarctation of the aorta, ventriculomegaly and thickened nuchal fold
|
陳持平(Chih-Ping Chen)*;(Yi-Yung Chen);(Schu-Rern Chern);(Peih-Shan Wu);(Jun-Wei Su);(Yu-Ting Chen);(Li-Feng Chen);(Wayseen Wang) |
| 中國醫藥大學 |
2012-12 |
Mosaic trisomy 2 at amniocentesis: prenatal diagnosis and molecular genetic analysis
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陳持平(Chih-Ping Chen)*;(Yi-Ning Su);(Schu-Rern Chern);(Yu-Ting Chen);(Peih-Shan Wu);(Jun-Wei Su);(Chen-Wen Pan);(Wayseen Wang) |
| 中國醫藥大學 |
2012-12 |
Prenatal diagnosis of an interstitial deletion of 10q (10q11.21->q21.1): array comparative genomic hybridization characterization and literature review
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陳持平(Chih-Ping Chen)*;(Yi-Ning Su);(Schu-Rern Chern);(Peih-Shan Wu);(Jun-Wei Su);(Dai-Dyi Town);(Wayseen Wang) |
| 中國醫藥大學 |
2012-12 |
Rapid diagnosis of trisomy 21 by array comparative genomic hybridization using uncultured amniocytes in a pregnancy with isolated ventriculomegaly in the fetus
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陳持平(Chih-Ping Chen)*;(Schu-Rern Chern);(Peih-Shan Wu);(Jun-Wei Su);(Li-Feng Chen);(Wayseen Wang) |
顯示項目 36-45 / 49 (共5頁)
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