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顯示項目 659211-659220 / 2349128 (共234913頁) << < 65917 65918 65919 65920 65921 65922 65923 65924 65925 65926 > >> 每頁顯示[10|25|50]項目
| 國家衛生研究院 |
2023-09-07 |
Perinatal dietary patterns and symptomatic depression: A prospective cohort study
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Chan, LC;Wang, HH;Wahlqvist, ML;Liu, CC;Liu, JY;Lee, MS |
| 中山醫學大學 |
2011 |
Perinatal Effects of Combined Use of Heroin, Methadone, and Amphetamine during Pregnancy and Quantitative Measurement of Metabolites in Hair
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Su, Pen-Hua; Chang, Yan-Zin; Yang, Chen; Ng, Yan-Yan; Chen, Jia-Yuh; Chen, Su-Chin |
| 中山醫學大學 |
2021 |
Perinatal Factors in Newborn Are Insidious Risk Factors for Childhood Autism Spectrum Disorders: A Population-based Study
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Lee, IC; Wang, YH; Chiou, JY; Wei, JCC |
| 中山醫學大學 |
2022-01 |
Perinatal Factors in Newborn Are Insidious Risk Factors for Childhood Autism Spectrum Disorders: A Population-based Study
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Inn-Chi Lee 1 2, Yu-Hsun Wang 3, Jeng-Yuan Chiou 4, James Cheng-Chung Wei 5 6 |
| 中國醫藥大學 |
2005 |
Perinatal finding and molecular cytogenetic analysis of de novo partial trisomy 16q (16q22.1→qter) and partial monosomy 20q (20q13.3→qter).
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陳持平(Chen CP,); (Lin SP,); 林齊強(Lin CC,); (Li YC,); (Chern SR,); (Chen WM,); (Lee CC,); 謝麗嬌(Hsieh LJ,) |
| 中國醫藥大學 |
2005 |
Perinatal findings and molecular cytogenetic analysis of de novo partial trisomy 16q (16q22.1 -> qter) and partial monosomy 20q (20q13.3 -> qter)
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Chen, CP; Lin, SP; Lin, CC; Li, YC; Chern, SR; Chen, WM; Lee, CC; Hsieh, LJ; Wang, WS |
| 中國醫藥大學 |
2005 |
Perinatal findings and molecular cytogenetic analysis of de novo partial trisomy 16q (16q22.1 -> qter) and partial monosomy 20q (20q13.3 -> qter)
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Chen, CP; Lin, SP; Lin, CC; Li, YC; Chern, SR; Chen, WM; Lee, CC; Hsieh, LJ; Wang, WS |
| 中國醫藥大學 |
2005 |
Perinatal findings of partial trisomy 13q (13q14.1 -> qter) resulting from paternal pericentric inversion of chromosome 13
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Chen, CP; Lin, SP; Lee, CC; Chen, WL; Chen, LF; Wang, WS |
| 亞洲大學 |
2017-02 |
Perinatal imaging findings and molecular genetic analysis of thanatophoric dysplasia type 1 in a fetus with a c.2419T>G ;p.Ter807Gly ;X807G mutation in FGFR3
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Wang, 陳馨文;Shin-Wen Chen;陳持平;Chih-Ping Chen;Liang-Kai Wa;Liang-Kai Wang;Schu-Rern Ch;Schu-Rern Chern;Pei-Chen Wu;Pei-Chen Wu;Yen-Ni Chen;Yen-Ni Chen;Chen-Ju Lin;Chen-Ju Lin;Wen-Ling Che;Wen-Ling Chen;Wayseen Wang;Wayseen |
| 中國醫藥大學 |
2007-09 |
Perinatal imaging findings of Galloway-Mowat syndrome
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陳持平(Chih-Ping Chen)* |
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