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Showing items 682851-682875 of 2349128 (93966 Page(s) Totally)
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| 亞洲大學 |
2010-03 |
Prenatal diagnosis of a 4.9-Mb deletion of 10q11.21->q11.23 by array comparative genomic hybridization
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陳持平;Chen, Chih-Ping;Su, Yi-Ning;Chern, Schu-Rern;Tsai, Fuu-Jen;Hsu, Chin-Yuan;Lee, Chen-Chi;Wang, Wayseen |
| 亞洲大學 |
2011-12 |
Prenatal diagnosis of a de novo 17p13.1 microduplication in a fetus with ventriculomegaly and lissencephaly
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陳持平;Chen, Chih-Ping |
| 中國醫藥大學 |
2014-12 |
Prenatal diagnosis of a de novo 9p terminal chromosomal deletion in a fetus with major congenital anomalies
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(Wen-Chien Hou);陳持平(Chih-Ping Chen);(Kwei-Shuai Hwang);(Ying-Chieh Chen);(Yu-Ju Lai);(Chau-Yang Tien);(Her-Young Su)* |
| 亞洲大學 |
2011-12 |
Prenatal diagnosis of a de novo interstitial deletion of chromosome 20q12 in a fetus with complex congenital heart defects, corpus callosum agenesis and intrauterine growth restriction
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陳持平;Chen, Chih-Ping |
| 中國醫藥大學 |
2011-12 |
Prenatal diagnosis of a de novo interstitial deletion of chromosome 20q12 in a fetus with complex congenital heart defects, corpus callosum agenesis and intrauterine growth restriction
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(Yi-Hui Lin);陳持平(Chih-Ping Chen)*;(Tze-Chien Chen);(Chun-Sen Hsu);(Szu-Yuan Chou);簡淑錦(Shu-Chin Chien) |
| 亞洲大學 |
2018-10 |
Prenatal diagnosis of a familial 15q11.2 (BP1-BP2) microdeletion encompassing TUBGCP5, CYFIP1, NIPA2 and NIPA1 in a fetus with ventriculomegaly, microcephaly and intrauterine growth restriction on prenatal ultrasound
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陳持平;Chen, Chih-Ping;Cha, Shu-Yuan;Chang, Shu-Yuan;Wa, Liang-Kai;Wang, Liang-Kai;Cha, Tung-Yao;Chang, Tung-Yao;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Chen, hin-Wen;Chen, hin-Wen;La, Shih-Ting;Lai, Shih-Ting;Chua, Tzu-Yun;Chuang, Tzu-Yun;Ya, Chien-Wen;Yang, Chien-Wen |
| 亞洲大學 |
2018-10 |
Prenatal diagnosis of a familial 1q21.1-q21.2 microdeletion in a fetus with polydactyly of left foot on prenatal ultrasound
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陳持平;Chen, Chih-Ping;Cha, Shu-Yuan;Chang, Shu-Yuan;Chen, Yen-Ni;Chen, Yen-Ni;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Che, Shin-Wen;Chen, Shin-Wen;La, Shih-Ting;Lai, Shih-Ting;Chua, Tzu-Yun;Chuang, Tzu-Yun;Ya, Chien-Wen;Yang, Chien-Wen;Chen, Li-Feng;Chen, Li-Feng |
| 亞洲大學 |
2018-10 |
Prenatal diagnosis of a familial 5p14.3-p14.1 deletion encompassing CDH18, CDH12, PMCHL1, PRDM9 and CDH10 in a fetus with congenital heart disease on prenatal ultrasound
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陳持平;Chen, Chih-Ping;Cha, Shu-Yuan;Chang, Shu-Yuan;Lin, Chen-Ju;Lin, Chen-Ju;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Che, Shin-Wen;Chen, Shin-Wen;Lai, hih-Ting;Lai, hih-Ting;Chua, Tzu-Yun;Chuang, Tzu-Yun;Chen, Wen-Lin;Chen, Wen-Lin;Ya, Chien-Wen;Yang, Chien-Wen |
| 國立臺灣大學 |
2004 |
Prenatal Diagnosis of a Fetus Affected with down Syndrome and Deletion 1p 36 Syndrome by Fluorescence in Situ Hybridization and Spectral Karyotyping
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謝聰哲; 葉光芃; 陳明; 王寶田; HSIEH, TSUNG-CHE; YEH, GUANG-PERNG; CHEN, MING; WANG, BAO-TYAN |
| 臺大學術典藏 |
2018-09-10T05:03:07Z |
Prenatal diagnosis of a fetus affected with down syndrome and deletion 1p36 syndrome by fluorescence in situ hybridization and spectral karyotyping
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Hsieh, L.-J.;Hsieh, T.-C.;Yeh, G.-P.;Lin, M.-I.;Chen, M.;Wang, B.B.-T.; MING CHEN |
| 國立臺灣大學 |
2012 |
Prenatal diagnosis of a fetus with a de novo trisomy 12p by array-comparative genomic hybridization (array-CGH)
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Hung, Chia-Cheng; Lin, Chia-Hui; Lin, Shin-Yu; Shin, Jin-Chung; Lee, Chien-Nan; Su, Yi-Ning; 林芯?; 蘇怡寧; 李建南; 林佳慧 |
| 臺大學術典藏 |
2018-09-10T09:27:32Z |
Prenatal diagnosis of a fetus with a de novo trisomy 12p by array-comparative genomic hybridization (array-CGH)
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Lee, Chien-Nan; Su, Yi-Ning; Shin, Jin-Chung; Lin, Chia-Hui; Lin, Shin-Yu; CHIEN-NAN LEE; SHIN-YU LIN; Hung, Chia-Cheng; 林芯?;蘇怡寧;李建南;林佳慧; Hung, Chia-Cheng;Lin, Chia-Hui;Lin, Shin-Yu;Shin, Jin-Chung;Lee, Chien-Nan;Su, Yi-Ning; Hung, C.-C. and Lin, C.-H. and Lin, S.-Y. and Shin, J.-C. and Lee, C.-N. and Su, Y.-N. |
| 臺大學術典藏 |
2020-02-12T04:05:56Z |
Prenatal diagnosis of a fetus with a de novo trisomy 12p by array-comparative genomic hybridization (array-CGH)
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Su Y.-N.;CHIEN-NAN LEE;Shin J.-C;Lin S.-Y;Lin C.-H;Hung C.-C; Hung C.-C; Lin C.-H; Lin S.-Y; Shin J.-C; CHIEN-NAN LEE; Su Y.-N. |
| 臺大學術典藏 |
2021-02-04T06:47:07Z |
Prenatal diagnosis of a fetus with distal 10q trisomy
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Chen C.-P.;Jin-Chung Shih;Lee C.-C.;Chen L.-F.;Wang W.;Wang T.-Y.; Chen C.-P.; JIN-CHUNG SHIH; Lee C.-C.; Chen L.-F.; Wang W.; Wang T.-Y. |
| 國立成功大學 |
2001-06 |
Prenatal diagnosis of a fetus with megacystis and monosomy 21
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Chang, Ling-Wei; Chen, Pei-Yi; Kuo, Pao-Lin; Chang, Fong-Ming |
| 中國醫藥大學 |
2006 |
Prenatal diagnosis of a micropenis in a male fetus with partial trisomy 12q (12q24.32->qter)and partial monosomy 21q(21q22.2->qter).
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陳持平(Chen CP,); 林齊強(Lin CC,); 李月君(Li YC,); 謝麗嬌(Hsieh LJ,) |
| 亞洲大學 |
2013-03 |
Prenatal diagnosis of a missense mutation of c.2279G>A, Gly760Glu in exon 37 of COL1A2 in a fetus with familial osteogenesis imperfecta type IV and favorable outcome
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陳持平;Chen, Chih-Ping;Li, Shuan-Pei;Lin, Shuan-Pei;Su, Yi-Ning;Su, Yi-Ning;Ch, Schu-Rern;Chern, Schu-Rern;Su, Jun-Wei;Su, Jun-Wei;Wang, Wayseen;Wang, Wayseen |
| 中國醫藥大學 |
2013-03 |
Prenatal diagnosis of a missense mutation of c.2279G>A, Gly760Glu in exon 37 of COL1A2 in a fetus with familial osteogenesis imperfecta type IV and favorable outcome
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陳持平(Chih-Ping Chen)*;(Shuan-Pei Lin);(Yi-Ning Su);(Schu-Rern Chern);(Jun-Wei Su);(Wayseen Wang) |
| 國立臺灣大學 |
1993 |
Prenatal Diagnosis of a Succenturiate Placenta:A Case Report
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Chang, Chung-Ching; Su, Chu'ng-Guei; 柯滄銘; Chang, Chung-Ching; Su, Chu'ng-Guei; Ko, Tsang-Ming |
| 國立成功大學 |
2003-02 |
Prenatal diagnosis of a triplet pregnancy complicated with one acardius in a patient with didelphys uterus using three-dimensional ultrasound
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Chang, Ling-Wei; Chang, Chiung-Hsin; Yu, Chen-Hsiang; Chang, Fong-Ming |
| 中國醫藥大學 |
2002 |
Prenatal diagnosis of abdominal lymphangioma
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Ho, M; Lee, CC; Lin, TY |
| 中國醫藥大學 |
2002-08 |
Prenatal diagnosis of abdominal lymphangioma
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何銘(Ming- Ho); 李建忠(C.C Lee); 林智一(Tze-Yi Lin) |
| 國立成功大學 |
2000-05 |
Prenatal diagnosis of alobar holoprosencephaly by two-dimensional and three-dimensional ultrasound
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Lai, Tsung-Hsuan; Chang, Chiung-Hsin; Yu, Chen-Hsiang; Kuo, Pao-Lin; Chang, Fong-Ming |
| 亞洲大學 |
2017-12 |
Prenatal diagnosis of an 8q22.2-q23.3 deletion associated with bilateral cleft lip and palate and intrauterine growth restriction on fetal ultrasound
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陳持平;Chen, Chih-Ping;Cha, Tung-Yao;Chang, Tung-Yao;Hung, Fang-Yu;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Che, Shin-Wen;Chen, Shin-Wen;La, Shih-Ting;Lai, Shih-Ting;Chua, Tzu-Yun;Chuang, Tzu-Yun;Lee, Chen-Chi;Wang, Wayseen |
| 國立臺灣大學 |
2005 |
Prenatal Diagnosis of an Acardiac Amorphous Twin and the Anomalous Co- Twin in a Monoamniotic Twin Pregnancy
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陳持平; 施景中; 陳樹人; 林靜宜; 王偉信; 曾岐元; CHEN, CHIH-PING; SHIH, JIN-CHUNG; CHERN, SCHU-RERN; LIN, CHING-YI; WANG, WAYSEEN; TZEN, CHIN-YUAN |
Showing items 682851-682875 of 2349128 (93966 Page(s) Totally)
<< < 27310 27311 27312 27313 27314 27315 27316 27317 27318 27319 > >>
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