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顯示項目 682736-682745 / 2349128 (共234913頁)
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每頁顯示[10|25|50]項目
| 亞洲大學 |
2009-09 |
PRENATAL DIAGNOSIS AND MOLECULAR ANALYSIS OF TRIPLOIDY IN A FETUS WITH INTRAUTERINE GROWTH RESTRICTION, RELATIVE MACROCEPHALY AND HOLOPROSENCEPHALY
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Chih-Ping Chen;Schu-Rern Chern;Fuu-Jen Tsai;Chin-Yuan Hsu;Kevin Ko;Wayseen Wang |
| 亞洲大學 |
2009-09 |
Prenatal diagnosis and molecular analysis of triploidy in a fetus with intrauterine growth restriction, relative macrocephaly and holoprosencephaly
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陳持平;Chen, Chih-Ping;Chern, Schu-Rern;Tsai, Fuu-Jen;Hsu, Chin-Yuan;Ko, Kevin;Wang, Wayseen |
| 亞洲大學 |
2009-09 |
PRENATAL DIAGNOSIS AND MOLECULAR ANALYSIS OF TRISOMY 13 MOSAICISM
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Chih-Ping Chen;Schu-Rern Chern;Fuu-Jen Tsai;Hung-Hung Lin;Chen-Wen Pan;Wayseen Wang |
| 亞洲大學 |
2009-09 |
Prenatal diagnosis and molecular analysis of trisomy 13 mosaicism
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陳持平;Chen, Chih-Ping;Chern, Schu-Rern;Tsai, Fuu-Jen;Lin, Hung-Hung;Pan, Chen-Wen;Wang, Wayseen |
| 中國醫藥大學 |
2005 |
Prenatal diagnosis and molecular cytogenetic analysis of partial monosomy 10q (10q25.3 -> qter) and partial trisomy 18q (18q23 -> qter) in a fetus associated with cystic hygroma and ambiguous genitalia
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Chen, CP; Chern, SR; Wang, TH; Hsueh, DW; Lee, CC; Town, DD; Wang, WS; Ko, TM |
| 中國醫藥大學 |
2014-12 |
Prenatal diagnosis and molecular cytogenetic characterization of a 1.07-Mb microdeletion at 5q35.2-q35.3 associated with NSD1 haploinsufficiency and Sotos syndrome
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陳持平(Chih-Ping Chen)*;(Chen-Ju Lin);(Schu-Rern Chern);(Yu-Peng Liu);(Yu-Ling Kuo);(Peih-Shan Wu);(Dai-Dyi Town);(Li-Feng Chen);(Chien-Wen Yang);(Wayseen Wang) |
| 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 a de novo 4.858-Mb microdeletion in 15q14 associated with ACTC1 and MEIS2 haploinsufficiency and tetrology of Fallot
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陳持平;Chen, Chih-Ping;*;Chen, Chen-Yu;Chen, Chen-Yu;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Chen, Yen-Ni;Chen, Yen-Ni;Che, Shin-Wen;Chen, Shin-Wen;Chen, Li-Feng;Chen, Li-Feng;Ya, Chien-Wen;Yang, Chien-Wen;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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Wang；, 陳持平；Chih-Ping Chen；*；Chen-Yu Chen；Chen-Yu Chen；Schu-Rern Ch；Schu-Rern Chern；Peih-Shan Wu；Peih-Shan Wu；Yen-Ni Chen；Yen-Ni Chen；Shin-Wen Che；Shin-Wen Chen；Li-Feng Chen；Li-Feng Chen；Chien-Wen Ya；Chien-Wen Yang；Wayseen Wang；Wayseen |
| 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) |
顯示項目 682736-682745 / 2349128 (共234913頁)
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每頁顯示[10|25|50]項目
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