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"su y n"的相关文件
显示项目 331-340 / 715 (共72页)
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| 臺大學術典藏 |
2020-05-24T05:47:51Z |
Fragile X syndrome carrier screening in pregnant women in Chinese Han population
|
Hung C.-C.; Lee C.-N.; Wang Y.-C.; Chen C.-L.; Lin T.-K.; Su Y.-N.; MING-WEI LIN; Kang J.; Tai Y.-Y.; Hsu W.-W.; Lin S.-Y. |
| 臺大學術典藏 |
2020-05-24T05:40:07Z |
Prenatal diagnosis of true diphallia and associated anomalies
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YI-AN TU; Su Y.-N.; Yang P.-K.; Shih J.-C. |
| 臺大學術典藏 |
2020-04-24T01:34:25Z |
Phenotypic analyses and mutation screening of the SLC26A4 and FOXI1 genes in 101 Taiwanese families with bilateral nonsyndromic enlarged vestibular aqueduct (DFNB4) or pendred syndrome
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Hsu C.-J.; Hwu W.-L.; Su Y.-N.; Yeh P.-L.; Chen P.-J.; Lu Y.-C.; Chen-Chi Wu |
| 臺大學術典藏 |
2020-04-24T01:34:24Z |
Preimplantation genetic diagnosis (embryo screening) for enlarged vestibular aqueduct due to SLC26A4 mutation
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Chen-Chi Wu; Lin S.-Y.; Su Y.-N.; Fang M.-Y.; Chen S.-U.; Hsu C.-J. |
| 臺大學術典藏 |
2020-04-24T01:34:23Z |
Mutation screening of the EYA1, SIX1, and SIX5 genes in an East Asian cohort with branchio-oto-renal syndrome
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Wang S.-H.; Chen-Chi Wu; Lu Y.-C.; Lin Y.-H.; Su Y.-N.; Hwu W.-L.; Yu I.-S.; Hsu C.-J. |
| 臺大學術典藏 |
2020-04-24T01:34:23Z |
Newborn genetic screening for hearing impairment: A preliminary study at a tertiary center
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Chen-Chi Wu; Hung C.-C.; Lin S.-Y.; Hsieh W.-S.; Tsao P.-N.; Lee C.-N.; Su Y.-N.; Hsu C.-J. |
| 臺大學術典藏 |
2020-04-24T01:34:19Z |
Newborn genetic screening for hearing impairment: a population-based longitudinal study
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Chen-Chi Wu; Tsai C.-H.; Hung C.-C.; Lin Y.-H.; Lin Y.-H.; Huang F.-L.; Tsao P.-N.; Su Y.-N.; Lee Y.L.; Hsieh W.-S.; Hsu C.-J. |
| 臺大學術典藏 |
2020-04-16T02:34:31Z |
A whole genome methylation analysis of systemic lupus erythematosus: Hypomethylation of the IL10 and IL1R2 promoters is associated with disease activity
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Lin, S.-Y.; Hsieh, S.-C.; Lin, Y.-C.; Ho, H.-N.; ERIC YAO-YU CHUANG; Lee, C.-N.; Tsai, M.-H.; Lai, L.-C.; Chuang, E.Y.; Chen, P.-C.; Hung, C.-C.; Chen, L.-Y.; Hsieh, W.S.; Niu, D.-M.; Su, Y.-N. |
| 臺大學術典藏 |
2020-03-23T07:52:30Z |
Mosaic paternal haploidy in a patient with pancreatoblastoma and Beckwith–Wiedemann spectrum
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Tsai W.-Y.; Lee N.-C.; Liu S.-Y.; Jong Y.-J.; Su Y.-N.; Chen M.; Yang Y.-L.; Chen H.-L.; Wu M.-Z.; Kuo K.-T.; WEN-HSI LIN; Shih J.-C.; Hwu W.-L.; Tung Y.-C.; Lee N.-C.;Tsai W.-Y.;Liu S.-Y.;Jong Y.-J.;Su Y.-N.;Chen M.;Chen H.-L.;Yang Y.-L.;Kuo K.-T.;Wu M.-Z.;WEN-HSI LIN;Shih J.-C.;Hwu W.-L.;Tung Y.-C.;Lee C.-T.; Lee C.-T. |
| 臺大學術典藏 |
2020-03-22T08:29:50Z |
Fragile X syndrome carrier screening in pregnant women in Chinese Han population
|
Su Y.-N.; Lin M.-W.; Jessica KANG; Tai Y.-Y.; Hsu W.-W.; Lin S.-Y.; Hung C.-C.; Lee C.-N.; Wang Y.-C.; Chen C.-L.; Lin T.-K. |
显示项目 331-340 / 715 (共72页)
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每页显示[10|25|50]项目
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