|
|
???tair.name??? >
???browser.page.title.author???
|
"陳持平 chen cp"???jsp.browse.items-by-author.description???
Showing items 1-14 of 14 (1 Page(s) Totally)
1
View [10|25|50] records per page
| 中國醫藥大學 |
2009-03 |
The p21 codon 31( *)C- and DRD2 codon 313( *)T-related genotypes/alleles, but not XRCC1 codon 399, hOGG1 codon 326, and DRD1-48 polymorphisms, are correlated with the presence of leiomyoma.
|
謝耀元(Hsieh Yao-Yuan); 張其真(Chang CC); 包大靝(Da-Tian Bau); 蔡輔仁(Fuu-Jen Tsai); 蔡長海(Tsai CH); 陳持平(Chen CP) |
| 中國醫藥大學 |
2009-03 |
The p21 codon 31( *)C- and DRD2 codon 313( *)T-related genotypes/alleles, but not XRCC1 codon 399, hOGG1 codon 326, and DRD1-48 polymorphisms, are correlated with the presence of leiomyoma.
|
謝耀元(Hsieh Yao-Yuan); 張其真(Chang CC); 包大 (Da-Tian Bau); 蔡輔仁(Fuu-Jen Tsai)*; 蔡長海(Tsai CH); 陳持平(Chen CP) |
| 中國醫藥大學 |
2007.09 |
Cytogenetic variability in the proportion of abnormal cells between the various tissues in prenatally detected mosaic tetrasomy 12p
|
陳持平(Chen CP)*; 蔡輔仁(Fuu-Jen Tsai); (Chern SR); (Lee CC); (Town DD); (Wang W) |
| 中國醫藥大學 |
2007.09 |
Cytogenetic variability in the proportion of abnormal cells between the various tissues in prenatally detected mosaic tetrasomy 12p
|
陳持平(Chen CP)*; 蔡輔仁(Fuu-Jen Tsai); (Chern SR); (Lee CC); (Town DD); (Wang W) |
| 中國醫藥大學 |
2007.05 |
Prenatal diagnosis of concomitant gallbladder hydrops and pyelectasis with spontaneous resolution.
|
陳持平(Chen CP)*; 劉玉鵬(Liu YP); 簡淑錦(Shu-Chin Chien); 王偉信(Wang W) |
| 中國醫藥大學 |
2006 |
Primary ovarian failure in a mentally retarded woman with a de novo unbalanced X;autosome translocation.
|
陳持平(Chen CP,); 林齊強(Lin CC,); 李月君(Li YC,); 謝麗嬌(Hsieh LJ,); (Lee CC,); (Wang MS) |
| 中國醫藥大學 |
2006 |
Prenatal diagnosis of low-level mosaicism for a small XIST-negative supernumerary ring X chromosome in a nondysmorphic male fetus.
|
陳持平(Chen CP,); (Lin SP,); 林齊強(Lin CC,); 李月君(Li YC,); 謝麗嬌(Hsieh LJ,); (Chern SR,); (Lee CC,); (Chen LF,); (Wang W.) |
| 中國醫藥大學 |
2006 |
Prenatal diagnosis of de novo t(2;18;14) (q33.1;q12.2; q31.2),dup(5)(q34q34), del(7)(p21.1p21.1), and del(10) (q25.3q25.3) and a review of the prenatally ascertained de novo apparently balanced complex and multiple chromosomal rearrangements
|
陳持平(Chen CP,); (Chern SR,); (Lee CC,); 林齊強(Lin CC,); 李月君(Li YC,); 謝麗嬌(Hsieh LJ,); (Chen WL,); (Wang W.) |
| 中國醫藥大學 |
2006 |
Spectral karyotyping and fluorescence in situ hybridization analysis of de novo partial trisomy 7p (7p21.2pter) and partial monosomy 12q (12q24.33qter)
|
陳持平(Chen CP,); (Lin SP,); 林齊強(Lin CC,); 李月君(Li YC,); 謝麗嬌(Hsieh LJ,); (Huang JK,); (Lee CC,); (Wang W..) |
| 中國醫藥大學 |
2006 |
Molecular cytogenetic analysis of de novo dup(5)(q35.2q35.3) and review of the literature of pure partial trisomy-5q.
|
陳持平(Chen CP,); (Lin SP,); 林齊強(Lin CC,); (Chen YJ,); (Chern SR,); 李月君(Li YC,); 謝麗嬌(Hsieh LJ,); (Lee CC,); (Wang W.) |
| 中國醫藥大學 |
2006 |
Prenatal diagnosis of a micropenis in a male fetus with partial trisomy 12q (12q24.32->qter)and partial monosomy 21q(21q22.2->qter).
|
陳持平(Chen CP,); 林齊強(Lin CC,); 李月君(Li YC,); 謝麗嬌(Hsieh LJ,) |
| 中國醫藥大學 |
2005 |
Spectral karyotyping and fluorescence in situ hybridization analysis of de novo partial duplication of Yq (Yq11.2→qter) and partial monosomy 5p (5p15.3→pter).
|
陳持平(Chen CP,); 林齊強(Lin CC,); 謝麗嬌(Hsieh LJ,) |
| 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).
|
陳持平(Chen CP,); 林齊強(Lin CC); 李月君(Li YC); 謝麗嬌(Hsieh LJ,) |
| 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).
|
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,) |
Showing items 1-14 of 14 (1 Page(s) Totally)
1
View [10|25|50] records per page
|
