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| 亞洲大學 |
2009-10 |
Association of TNF-alpha gene polymorphisms with systemic lupus erythematosus in Taiwanese patients
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Lin, YJ (Lin, Y-J); Chen, RH (Chen, R-H); Wan, L (Wan, L.); Sheu, JJC (Sheu, J. J-C); Huang, CM (Huang, C-M); Lin, CW (Lin, C-W); Chen, SY (Chen, S-Y); Lai, CH (Lai, C-H); Lan, YC (Lan, Y-C); Hsueh, KC (Hsueh, K-C); Tsai, CH (Tsai, C-H); Lin, TH (Lin, T-H); Huang, YM (Huang, Y-M); Chao, K (Chao, K.); Chen, DY (Chen, D-Y); Tsai, FJ (Tsai, F-J) |
| 亞洲大學 |
2009-02 |
HLA-E Gene Polymorphism Associated With Susceptibility to Kawasaki Disease and Formation of Coronary Artery Aneurysms
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Lin, YJ (Lin, Y. -J.); Wan, L (Wan, L.); Wu, JY (Wu, J. -Y.); Sheu, JJC (Sheu, J. J. -C.); Lin, CW (Lin, C. -W.); Lan, YC (Lan, Y. -C.); Lai, CH (Lai, C. -H.); Hung, CH (Hung, C. -H.); Tsai, Y (Tsai, Y.); Tsai, CH (Tsai, C. -H.); Lin, TH (Lin, T. -H.); Lin, JG (Lin, J. -G.); Hsueh, KC (Hsueh, K. -C.); Huang, YM (Huang, Y. -M.); Chang, JS (Chang, J. -S.); Tsai, FJ (Tsai, F. -J.) |
| 亞洲大學 |
2009 |
PRENATAL DIAGNOSIS OF PARTIAL TRISOMY 14q (14q31.1 -> qter) AND PARTIAL MONOSOMY 5p (5p13.2 -> pter) ASSOCIATED WITH POLYHYDRAMNIOS, SHORT LIMBS, MICROPENIS AND BRAIN MALFORMATIONS
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Chen, CP (Chen, C-P); Chern, SR (Chern, S. -R.); Tsai, FJ (Tsai, F-J.); Lee, CC (Lee, C. -C.); Chen, LE (Chen, L. -E); Wang, W (Wang, W.) |
| 亞洲大學 |
2008-03 |
Association of vascular endothelial growth factor C-634 G polymorphism in Taiwanese children with Kawasaki disease
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Hsueh, KC (Hsueh, K. -C.); Lin, YJ (Lin, Y. -J.); Chang, JS (Chang, J. -S.); Wan, L (Wan, L.); Tsai, YH (Tsai, Y. -H.); Tsai, CH (Tsai, C. -H.); Chen, CP (Chen, C. -P.); Tsai, FJ (Tsai, F. -J.) |
| 亞洲大學 |
2008-01 |
Evaluation of transforming growth factor and vascular endothelial growth factor polymorphisms in Taiwan Chinese patients with pterygium
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Bau, DT (Bau, D. -T.); Chiang, CC (Chiang, C. -C.); Tsai, YY (Tsai, Y. -Y.); Lee, CC (Lee, C. -C.); Tsai, Y (Tsai, Y.); Lin, CC (Lin, C. -C.); Tsai, CH (Tsai, C. -H.); Tsai, FJ (Tsai, F. -J.) |
| 亞洲大學 |
2008 |
Craniosynostosis and congenital tracheal anomalies in an infant with Pfeiffer syndrome carrying the W290CFGFR2 mutation
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Chen, CP (Chen, C. -P.); Lin, SP (Lin, S. -P.); Su, YN (Su, Y. -N.); Chen, SC (Chen, S. -C.); Tsai, FJ (Tsai, F. -J.); Wang, W (Wang, W.) |
| 亞洲大學 |
2008 |
Transient abnormal myelopoiesis of mosaic trisomy 21 presenting fetoplacental cytogenetic discrepancy, hepatosplenomegaly, oligohydramios and abnormal hematological findings
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Chen, CP (Chen, C. -P.); Lin, SP (Lin, S. -P.); Tsai, FJ (Tsai, F. -J.); Lin, HH (Lin, H. -H.); Chern, SR (Chern, S. -R.); Chuang, CK (Chuang, C. -K.); Lee, CC (Lee, C. -C.); Wang, W (Wang, W.) |
| 亞洲大學 |
2008 |
Occipital encephalocele associated with iniencephaly mimicking an unilateral nuchal tumor on prenatal ultrasound
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Chen, CP (Chen, C. -P.); Hwu, YM (Hwu, Y. -M.); Tsai, FJ (Tsai, F. -J.); Wang, W (Wang, W.) |
Showing items 1-8 of 8 (1 Page(s) Totally)
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