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Showing items 1-12 of 12 (1 Page(s) Totally)
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| 亞洲大學 |
2016-06 |
Molecular cytogenetic characterization of inv dup del(8p) in a fetus associated with ventriculomegaly, hypoplastic left heart, polyhydramnios and intestinal obstruction
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Chen)*, 陳持平(Chih-Ping;Ko), Tsang-Ming K(Tsang-Ming;Huang), Wen-Chu Huan(Wen-Chu;Chern), Schu-Rern Ch(Schu-Rern;Wu), Peih-Shan Wu(Peih-Shan;Chen), Yen-Ni Chen(Yen-Ni;Chen), Shin-Wen Che(Shin-Wen;Lee), Chen-Chi Lee(Chen-Chi;(Chen-Wen Pan,);Wang), Wayseen Wang(Wayseen |
| 亞洲大學 |
2016-06 |
Prenatal diagnosis of mosaic small supernumerary marker chromosome 17 associated with ventricular septal defect, developmental delay and speech delay
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Chen)*, 陳持平(Chih-Ping;Chiang), Sheng Chiang(Sheng;Wang), Kung-Liahng(Kung-Liahng;Cho), Fu-Nan Cho(Fu-Nan;Chen), Ming Chen(Ming;Chern), Schu-Rern Ch(Schu-Rern;Wu), Peih-Shan Wu(Peih-Shan;Chen), Yen-Ni Chen(Yen-Ni;(Shin-Wen Chen,);(Shun-Ping Chang,);Chen), Weu-Lin Chen(Weu-Lin;Wang), Wayseen Wang(Wayseen |
| 亞洲大學 |
2016-06 |
22q13 deletion syndrome in a fetus associated with microtia, hemivertebrae and congenital heart defects on prenatal ultrasound
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Chen)*, 陳持平(Chih-Ping;Chang), Tung-Yao Cha(Tung-Yao;Wang), Liang-Kai Wa(Liang-Kai;Chern), Schu-Rern Ch(Schu-Rern;Wu), Peih-Shan Wu(Peih-Shan;Chen), Yen-Ni Chen(Yen-Ni;Chen), Shin-Wen Che(Shin-Wen;Chen), Weu-Lin Chen(Weu-Lin;Wang), Wayseen Wang(Wayseen |
| 亞洲大學 |
2016-04 |
Prenatal diagnosis and molecular cytogenetic characterization of a de novo 4.858-Mb microdeletion in 15q14 associated with ACTC1 and MEIS2 haploinsufficiency and tetrology of Fallot
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Chen)*, 陳持平(Chih-Ping;Chen), Chen-Yu Chen(Chen-Yu;Chern), Schu-Rern Ch(Schu-Rern;Wu), Peih-Shan Wu(Peih-Shan;Chen), Yen-Ni Chen(Yen-Ni;Chen), Shin-Wen Che(Shin-Wen;Chen), Li-Feng Chen(Li-Feng;Yang), Chien-Wen Ya(Chien-Wen;Wang), Wayseen Wang(Wayseen |
| 亞洲大學 |
2016-04 |
Prenatal diagnosis and molecular cytogenetic characterization of low-level true mosaicism for trisomy 21 using uncultured amniocytes
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Chen)*, 陳持平(Chih-Ping;Wang), Yeou-Lih Wan(Yeou-Lih;Chern), Schu-Rern Ch(Schu-Rern;Wu), Peih-Shan Wu(Peih-Shan;Chen), Yen-Ni Chen(Yen-Ni;Chen), Shin-Wen Che(Shin-Wen;Chen), Li-Feng Chen(Li-Feng;Lee), Meng-Shan Le(Meng-Shan;Yang), Chien-Wen Ya(Chien-Wen;Wang), Wayseen Wang(Wayseen |
| 亞洲大學 |
2016-04 |
Prenatal diagnosis and molecular cytogenetic characterization of de novo partial monosomy 3p (3p26.3->pter) and partial trisomy 16q (16q23.1->qter)
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Chen)*, 陳持平(Chih-Ping;Hung), Fang-Yu Hung(Fang-Yu;Chern), Schu-Rern Ch(Schu-Rern;Wu), Peih-Shan Wu(Peih-Shan;Chen), Yen-Ni Chen(Yen-Ni;Chen), Shin-Wen Che(Shin-Wen;Lee), Chen-Chi Lee(Chen-Chi;Wang), Wayseen Wang(Wayseen |
| 亞洲大學 |
2016-04 |
Prenatal diagnosis of low-level mosaicism for trisomy 2 associated with a favorable pregnancy outcome
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Chen)*, 陳持平(Chih-Ping;Ko), Tsang-Ming K(Tsang-Ming;Chern), Schu-Rern Ch(Schu-Rern;Wu), Peih-Shan Wu(Peih-Shan;Chen), Yen-Ni Chen(Yen-Ni;Chen), Shin-Wen Che(Shin-Wen;Chen), Li-Feng Chen(Li-Feng;Yang), Chien-Wen Ya(Chien-Wen;Wang), Wayseen Wang(Wayseen |
| 亞洲大學 |
2016-02 |
Prenatal diagnosis of 22q11.2 deletion syndrome associated with right aortic arch, left ductus arteriosus, cardiomegaly, and pericardial effusion
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Chen), Yen-Ni Chen(Yen-Ni;陳持平*;Ko), Tsang-Ming K(Tsang-Ming;Wang), Liang-Kai Wa(Liang-Kai;Wu), Pei-Chen Wu(Pei-Chen;Chang), Tung-Yao Cha(Tung-Yao;Wu), Peih-Shan Wu(Peih-Shan;Yang), Chien-Wen Ya(Chien-Wen;Wang), Wayseen Wang(Wayseen |
| 亞洲大學 |
2015-10 |
Prenatal diagnosis and array comparative genomic hybridization characterization of interstitial deletions of 8q23.3-q24.11 and 8q24.13 associated with Langer-Giedion syndrome and Cornelia de Lange syndrome and haploinsufficiency of TRPS1, RAD21 and EXT1
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陳持平*;Lin), Ming-Huei Li(Ming-Huei;Chen), Yi-Yung Chen(Yi-Yung;Chern), Schu-Rern Ch(Schu-Rern;Chen), Yen-Ni Chen(Yen-Ni;Wu), Peih-Shan Wu(Peih-Shan;Pan), Chen-Wen Pan(Chen-Wen;Lee), Meng-Shan Le(Meng-Shan;Wang), Wayseen Wang(Wayseen |
| 亞洲大學 |
2015-08 |
Mosaic trisomy 15 at amniocentesis: prenatal diagnosis, molecular genetic analysis and literature review
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陳持平*;Chern), Schu-Rern Ch(Schu-Rern;Chen), Yen-Ni Chen(Yen-Ni;Wu), Peih-Shan Wu(Peih-Shan;Yang), Chien-Wen Ya(Chien-Wen;Chen), Li-Feng Chen(Li-Feng;Wang), Wayseen Wang(Wayseen |
| 亞洲大學 |
2015-08 |
Pregnancy with de novo 9q34.3 microdeletion and Kleefstra syndrome in the fetus may be associated with an abnormal maternal serum screening result
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陳持平*;Lin), Shuan-Pei Li(Shuan-Pei;Li), Hui-Bo Li(Hui-Bo;Chen), Yen-Ni Chen(Yen-Ni;Wang), Wayseen Wang(Wayseen |
| 亞洲大學 |
2015-06 |
Distal 3p duplication and terminal 7q deletion associated with nuchal edema and cyclopia in a fetus and a review of the literature
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陳持平*;Huang), Ming-Chao Hu(Ming-Chao;Chern), Schu-Rern Ch(Schu-Rern;Kuo), Yu-Ling Kuo(Yu-Ling;Chen), Yen-Ni Chen(Yen-Ni;Wu), Peih-Shan Wu(Peih-Shan;Chen), Li-Feng Chen(Li-Feng;Pan), Chen-Wen Pan(Chen-Wen;Wang), Wayseen Wang(Wayseen |
Showing items 1-12 of 12 (1 Page(s) Totally)
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