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"ming chen"
Showing items 116-125 of 141 (15 Page(s) Totally) << < 6 7 8 9 10 11 12 13 14 15 > >> View [10|25|50] records per page
| 中國醫藥大學 |
2011-12 |
A de novo duplication of chromosome 21q22.11->qter associated with Down syndrome: prenatal diagnosis, molecular cytogenetic characterization and fetal ultrasound findings
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陳持平(Chih-Ping Chen)*;(Hsu-Kuaing Huang);(Pei-Ying Lin);(Yi-Ning Su);(Ming Chen);蔡輔仁(Fuu-Jen Tsai);(Pei-Chen Wu);(Schu-Rern Chern);(Yu-Ting Chen);(Chen-Chi Lee);(Wayseen Wang) |
| 中國醫藥大學 |
2011-12 |
A 20.5-Mb germline deletion of 13q13.1->q14.3 and somatic mutations of the RB1 gene in an 8-year-old girl with unilateral retinoblastoma, developmental delay and mental retardation
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陳持平(Chih-Ping Chen)*;(Ling-Yuh Kao);(Yi-Ning Su);(Ming Chen);(Shueen-Dyh Chang);(Wayseen Wang) |
| 中國醫藥大學 |
2011-09 |
Mosaic supernumerary r(1)(p13.2q23.3) in a 10-year-old girl with epilepsy, facial asymmetry, psychomotor retardation, kyphoscoliosis, dermatofibrosarcoma and multiple exostoses
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陳持平(Chih-Ping Chen)*;(Shuan-Pei Lin);(Ming Chen);(Yi-Ning Su);(Schu-Rern Chern);(Tao-Yeuan Wang);(Yu-Peng Liu);蔡輔仁(Fuu-Jen Tsai);(Chen-Chi Lee);(Yen-Jiun Chen);(Wayseen Wang) |
| 中國醫藥大學 |
2011-09 |
Prenatal diagnosis of mosaic trisomy 8: clinical report and literature review
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陳持平(Chih-Ping Chen)*;(Ming Chen);(Yi-Ju Pan);(Yi-Ning Su);(Schu-Rern Chern);蔡輔仁(Fuu-Jen Tsai);(Yu-Ting Chen);(Wayseen Wang) |
| 中國醫藥大學 |
2011-09 |
Prenatal diagnosis and molecular cytogenetic characterization of a mosaic derivative Y chromosome derived from a de novo unbalanced reciprocal Yq;13q translocation
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陳持平(Chih-Ping Chen)*;(Yi-Ning Su);(Ming Chen);(Jain-Pei Huang);蔡輔仁(Fuu-Jen Tsai);(Pei-Chen Wu);(Wen-Lin Chen);(Wayseen Wang) |
| 中國醫藥大學 |
2010-12 |
Chromosome 1p36 deletion syndrome: prenatal diagnosis, molecular cytogenetic characterization and fetal ultrasound findings
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陳持平(Chih-Ping Chen)*; (Ming Chen); (Yi-Ning Su); (Chin-Yuan Hsu); 蔡輔仁(Fuu-Jen Tsai); (Schu-Rern Chern); (Pei-Chen Wu); (Chen-Chi Lee); (Wayseen Wang) |
| 中國醫藥大學 |
2010-12 |
Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 8
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陳持平(Chih-Ping Chen)*; (Ming Chen); (Tsang-Ming Ko); (Gwo-Chin Ma); 蔡輔仁(Fuu-Jen Tsai); (Ming-Song Tsai); (Pei-Chen Wu); (Chen-Chi Lee); (Li-Feng Che); (Wayseen Wang) |
| 中國醫藥大學 |
2010-09 |
Prenatal diagnosis and molecular cytogenetic characterization of de novo partial trisomy 7p (7p15.3->pter) and partial monosomy 13q (13q33.3->qter) associated with Dandy-Walker malformation, abnormal skull development and microcephaly
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陳持平(Chih-Ping Chen)*; (Ming Chen); (Yi-Ning Su); 蔡輔仁(Fuu-Jen Tsai); (Schu-Rern Chern); (Chin-Yuan Hsu); (Pei-Chen Wu); (Dai-Dyi Town); (Dong-Jay Lee); (Gwo-Chin Ma); (Wayseen Wang) |
| 亞洲大學 |
2010-03 |
Ventriculomegaly, intrauterine growth restriction and congenital heart defects as salient prenatal sonographic findings of Miller-Dieker lissencephaly syndrome associated with monosomy 17p (17p13.2->pter) in a fetus
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Chih-Ping Chen;Yu-Peng Liu;Shaun-Pei Lin;Ming Chen;Fuu-Jen Tsai;Yu-Ting Chen;Li-Feng Chen;Jonathan Kwei Hwang;Wayseen Wang |
| 中國醫藥大學 |
2010-03 |
Ventriculomegaly, intrauterine growth restriction and congenital heart defects as salient prenatal sonographic findings of Miller-Dieker lissencephaly syndrome associated with monosomy 17p (17p13.2->pter) in a fetus
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陳持平(Chih-Ping Chen)*; (Yu-Peng Liu); (Shuan-Pei Lin); (Ming Chen); 蔡輔仁(Fuu-Jen Tsai); (Yu-Ting Chen); (Li-Feng Chen); (Jonathan Kwei Hwang); (Wayseen Wang) |
Showing items 116-125 of 141 (15 Page(s) Totally) << < 6 7 8 9 10 11 12 13 14 15 > >> View [10|25|50] records per page
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