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Showing items 682951-682960 of 2349128 (234913 Page(s) Totally)
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| 國立成功大學 |
2012-12 |
Prenatal diagnosis of fetal multicystic dysplastic kidney in the era of three-dimensional ultrasound: 10-year experience
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Hsu, PY (Hsu, Pei-Yang); Yu, CH (Yu, Chen-Hsiang); Lin, K (Lin, Kang); Cheng, YC (Cheng, Yueh-Chin); Chang, CH (Chang, Chiung-Hsin); Chang, FM (Chang, Fong-Ming) |
| 國立成功大學 |
2002-07 |
Prenatal diagnosis of fetal multicystic dysplastic kidney with two-dimensional and three-dimensional ultrasound
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Chang, Ling-Wei; Chang, Fong-Ming; Chang, Chiung-Hsin; Yu, Chen-Hsiang; Cheng, Yueh-Chin; Chen, Hsi-Yao |
| 國立臺灣大學 |
1991 |
Prenatal Diagnosis of Fetal Nuchal Cord Coiling with Color Doppler Imaging:A Case Report
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Lee, Chien-Nan; 謝豐舟; 何弘能; Tsai, Yieh-Loong; 柯滄銘; 陳皙堯; Kao, Miao-Lin; Lee, Chien-Nan; 謝豐舟; 何弘能; Tsai, Yieh-Loong; 柯滄銘; Chen, Hsi-Yao; Kao, Miao-Lin |
| 亞洲大學 |
201407 |
Prenatal diagnosis of fetal omphalocele by ultrasound: a comparison of two centuries
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Anonymous |
| 國立成功大學 |
2013-06 |
Prenatal diagnosis of fetal omphalocele by ultrasound: A comparison of two centuries
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Liang, Yu-Ling; Kang, Lin; Tsai, Pei-Ying; Cheng, Yueh-Chin; Ko, Huei-Chen; Chang, Chiung-Hsin; Chang, Fong-Ming |
| 中國醫藥大學 |
2007-10 |
Prenatal diagnosis of Fryns syndrome associated with a microdeletion at 8p23.1
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陳持平(Chih-Ping Chen)* |
| 臺大學術典藏 |
2022-03-10T07:59:00Z |
Prenatal diagnosis of Hb H disease due to compound heterozygosity for South?East Asian deletion and Hb constant spring by polymerase chain reaction
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Ko T.?M.; LI-HUI TSENG; Hsieh F.?J.; Lee T.?Y. |
| 國立臺灣大學 |
1993 |
Prenatal Diagnosis of HbH Disease Due to Compound Heterozygosity for Southeast Asian Deletion and Hb Constant Spring by Polymerase Chain Reaction
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柯滄銘; Tseng, Li-Hui; 謝豐舟; Lee, Tzu-Yao; Ko, Tsang-Ming; Tseng, Li-Hui; Hsieh, Fon-Jou; Lee, Tzu-Yao |
| 國立臺灣大學 |
1990 |
Prenatal Diagnosis of Hemophilia A by DNA Analysis on Chorionic Villi
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柯滄銘; Shen, Ming-Ching; 謝豐舟; Lee, Tzu-Yao; Ko, Tsang-Ming; Shen, Ming-Ching; Hsieh, Fon-Jou; Lee, Tzu-Yao |
| 國立成功大學 |
2003-02 |
Prenatal diagnosis of holoprosencephaly in two fetuses with der (7)t(1;7)(q32;q32)pat inherited from the father with double translocations
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Chuang, Louise; Kuo, Pao-Lin; Yang, Hsiao-Bai; Chien, Chung-Ho; Chen, Pei-Yi; Chang, Chiung-Hsin; Chang, Fong-Ming |
Showing items 682951-682960 of 2349128 (234913 Page(s) Totally)
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