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Taiwan Academic Institutional Repository >
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"wang ws"
Showing items 11-30 of 30 (2 Page(s) Totally)
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| 中國醫藥大學 |
2005 |
Spectral karyotyping, fluorescence in situ hybridization and molecular genetic analysis of de novo partial trisomy 7p (7p15.1 -> pter) and partial monosomy 9p (9p22 -> pter)
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Chen, CP; Lin, SP; Lin, CC; Li, YC; Hsieh, LJ; Chern, SR; Lee, CC; Chen, YJ; Wang, WS |
| 中國醫藥大學 |
2005 |
Prenatal diagnosis of an acardiac amorphous twin and the anomalous co-twin in a monoamniotic twin pregnancy
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Chen, CP; Shih, JC; Chang, TY; Chern, SR; Lin, CY; Wang, WS; Tzen, CY |
| 中國醫藥大學 |
2005 |
Contribution of ultrafast magnetic resonance imaging in prenatal diagnosis of sonographically undetected cerebral tuberous sclerosis associated with cardiac rhabdomyomas
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Chen, CP; Liu, YP; Huang, JK; Chang, TY; Chen, MR; Chiu, NC; Wang, WS |
| 中國醫藥大學 |
2005 |
Prenatal magnetic resonance imaging of Galloway-Mowat syndrome
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Chen, CP; Chang, TY; Lin, SP; Huang, JK; Tsai, JD; Chiu, NC; Wang, WS |
| 中國醫藥大學 |
2005 |
Recurrent short-rib polydactyly syndrome: prenatal three-dimensional ultrasound findings and associations with congenital high airway obstruction and pyelectasia
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Chen, CP; Shih, JC; Tzen, CY; Lin, YH; Wang, WS |
| 中國醫藥大學 |
2005 |
Prenatal diagnosis of de novo partial trisomy 13q (13q22 -> qter) and partial monosomy 8p (8p23.3 -> pter) associated with holoprosencephaly, premaxillary agenesis, hexadactyly, and a hypoplastic left heart
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Chen, CP; Chern, SR; Hsu, CY; Lee, CC; Lee, MS; Wang, WS |
| 中國醫藥大學 |
2005 |
A paternally derived inverted duplication of distal 14q with a terminal 14q deletion
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Chen, CP; Chern, SR; Lin, SP; Lin, CC; Li, YC; Wang, TH; Lee, CC; Pan, CW; Hsieh, LJ; Wang, WS |
| 中國醫藥大學 |
2005 |
A comparison of maternal age, sex ratio and associated major anomalies among fetal trisomy 18 cases with different cell division of error
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Chen, CP; Chern, SR; Tsai, FJ; Lin, CY; Lin, YH; Wang, WS |
| 中國醫藥大學 |
2005 |
Prenatal diagnosis and molecular cytogenetic analysis of partial monosomy 10q (10q25.3 -> qter) and partial trisomy 18q (18q23 -> qter) in a fetus associated with cystic hygroma and ambiguous genitalia
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Chen, CP; Chern, SR; Wang, TH; Hsueh, DW; Lee, CC; Town, DD; Wang, WS; Ko, TM |
| 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 |
Prenatal imaging of limb-body wall complex by magnetic resonance imaging
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Chen, CP; Cheng, SJ; Lin, YH; 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 |
| 中國醫藥大學 |
2005 |
Recurrent fetal pyelectasis in a family with fetuses associated with partial trisomy 10q (10q24.1 -> qter)
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Chen, CP; Chang, TY; Tzen, CY; Wang, WS; Lee, CC |
| 中國醫藥大學 |
2005 |
Prenatal diagnosis of concomitant alobar holoprosencephaly and caudal regression syndrome associated with maternal diabetes
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Chen, CP; Chen, CY; Lin, CY; Shaw, SW; Wang, WS; Tzen, CY |
| 中國醫藥大學 |
2005 |
Prenatal three-dimensional/four-dimensional sonographic demonstration of facial dysmorphisms associated with holoprosencephaly
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Chen, CP; Shih, JC; Hsu, CY; Chen, CY; Huang, JK; Wang, WS |
| 中國醫藥大學 |
2005 |
Prenatal diagnosis of de novo proximal interstitial deletion of 9q and review of the literature of uncommon aneuploidies associated with increased nuchal translucency
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Chen, CP; Chern, SR; Chang, TY; Chen, WL; Chen, LF; Wang, WS; Chen, HEC |
| 中國醫藥大學 |
2003 |
Prenatal identification of a G338E mutation in FGFR2 in a fetus without sonographic appearance of craniosynostosis
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Chen, CP; Chern, SR; Lin, SP; Wang, WS; Tsai, FJ |
| 國家衛生研究院 |
1999-06-15 |
Fulminant hepatitis is significantly increased in hepatitis B carriers after allogeneic bone marrow transplantation
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Chen, PM; Chiou, TJ; Fan, FS; Liu, JM; Hsieh, RK; Yen, CC; Wang, WS; Liu, JH |
| 中國醫藥大學 |
1997 |
Molecular analysis of survival motor neuron (SMN) and neuronal apoptosis inhibitory protein (NAIP) genes of spinal muscular atrophy patients and their parents
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Chang, JG; Jong, YJ; Lin, SP; Soong, BW; Tsai, CH; Yang, TY; Chang, CP; Wang, WS |
Showing items 11-30 of 30 (2 Page(s) Totally)
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